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Recalls affecting Kansas

Data last updated: September 10, 2026 at 1:16 PM UTC

16,731 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
UnclassifiedUndeclaredAnnounced September 4, 2026

Business Pill, Branch Manager for Mendietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

Full report
Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.

Company contact: (321) 341-9501 · SupplxRecall@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaAnnounced September 4, 2026

Foods AliveMoringa Leaf Powder

Potential to be contaminated with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

B. Braun0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

Full report
Drugs

Recalling firm: B. Braun Medical Inc.

“On September 3, 2026 firm updated their press release to include additional contaminants.” FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron…

Company contact: recalls@bbraunusa.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusE. coliAnnounced September 3, 2026

Great ValueOrganic Triple Berry Blend

Possible E. Coli Contamination

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Frutas y Hortalizas del Sur S.A.

September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145) .

Company contact: Info.foodsafety@comfrut.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

American Regent, Inc.Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Presence of particulate matter and lack of sterility assurance

Full report
Food & Beverages

Recalling firm: American Regent, Inc.

FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility.

View FDA’s announcement (opens in a new tab)
UnclassifiedAllergenMilkUndeclaredAnnounced August 31, 2026

Little TemptationsChocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

Full report
Food & BeveragesAllergens

Recalling firm: Crystal Temptations

Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

View FDA’s announcement (opens in a new tab)
UnclassifiedUndeclaredAnnounced August 31, 2026

LipofitLipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

Full report
Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.

Company contact: (954) 305-1004 · yandrydy@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced August 31, 2026

KofinasGarlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

Full report
Food & BeveragesIngredients

Recalling firm: LMSI LLC

Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaE. coliAnnounced August 29, 2026

Everything SproutsRobust Radish Mix, 5oz Cups

Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.

Company contact: everythingsproutsmn@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaAnnounced August 29, 2026

MartinaMangoes

Potential contamination with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)
Wording
UnclassifiedRisk not yet known
Medical deviceRecalled February 4, 2026

Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S Model/Catalog Number (REF): 00516 Product Description: The STA - Liatest Free Protein S kits are intended for use on STA-R and STA Compact for the quantitative antigenic assay of free protein S in human citrated plasma by the immuno-turbidimetric method. Component: Not Applicable

The potential of out-of-range results and an underestimation of the free protein S level in normal patient plasmas. The defect only affects normal-range values.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98394
Lot/product code:
Model/Catalog Number (REF): 00516; UDI: (1) (01)03607450005165(11)241001(17)260131(10)271971(241)00516, (2) (01)03607450005165(11)250221(17)260531(10)272859(241)00516, (3) (01)03607450005165(11)250306(17)260630(10)273018(241)00516, (4) (01)03607450005165(11)250430(17)260831(10)273426(241)00516; Lot numbers: (1) 271 971, (2) 272 859, (3) 273 018, (4) 273 426; Lot Code: 271 971 (01)03607450005165(11)241001(17)260131(10)271971(241)00516
Recalling firm:
Diagnostica Stago, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 4, 2026

The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS). Model Number: LVP-0004.

Potential for the Cassette Loading Lever to break.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98699
Lot/product code:
Model Number: LVP-0004. UDI-DI: 00811505030320
Recalling firm:
Fresenius Kabi USA, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 4, 2026

React Health PHOENIX 5L Oxygen Concentrator

Devices which did not meet internal quality specifications were inadvertently distributed.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98563
Lot/product code:
UDI 06934726614439-250623-MZJ5S713971, Serial Number MZJ5S713971; UDI 06934726614439-250623-MZJ5S714009, Serial Number MZJ5S714009
Recalling firm:
3B Medical, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled February 4, 2026

Dexamethasone Sodium Phosphate Injection, USP, 100 mg/ 10 mL, (10 mg/mL), 10x10 mL Multiple Dose Vials, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873, NDC carton: 70069-025-10; NDC vial: 70069-025-01

Failed Impurities/Degradation Specifications - OOS impurities result observed during long term stability testing at product expiry (24 months) were above specs for these impurities: Dexamethasone Sodium Phosphate EP impurity G (Impurity RU 49336) and dexamethasone formate.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0398-2026
Lot/product code:
Lot #: A240421, Exp 07/31/2026
Recalling firm:
SOMERSET THERAPEUTICS LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled February 3, 2026

Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset, Net Wt., 1 fl oz (30 ml) liquid dietary supplement, Glass bottle with dropper cap. (Individual 1 fl oz bottles (not sold in case lots)

Label declares bovine colostrum but does not declare milk allergen.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
H-0537-2026
Lot/product code:
LOT: 0528D911 Expiration Date: May 2028
Recalling firm:
Pure Solutions, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 3, 2026

Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05

Impactor handle may be missing cross-pin

Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98376
Lot/product code:
Lot Code: Part Number: 321-09-05 UDI-DI: 10885862557674 Lot Number: All (Please refer to Attachment 1 - Product Information Spreadsheet for details)
Recalling firm:
Exactech, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 3, 2026

Imactis CT-Navigation System, stereotaxic accessory for Computer Tomography (CT), systems, Model Numbers E85101LA and E85101LP

There is a potential issue that can lead to discordance between the simulated needle trajectory/tip position and the actual needle trajectory/tip position.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98447
Lot/product code:
HIBC: +B681J02000; E85101LA: IMB-22-013 IMB-24-013 IMB-23-006 IMB-24-001 IMB-24-016 IMB-24-018 IMB-24-007 IMB-21-001 IMB-23-004 IMB-24-015 IMB-22-014 IMB-22-011 IMB-21-008 IMB-22-010 IMB-23-003 IMB-22-002 IMB-16-005 IMB-16-002 IMB-17-007 IMB-21-003 IMB-16-003 IMB-18-006 IMB-16-006 IMB-19-014 IMB-23-007 IMB-19-011 IMB-24-011 IMB-15-001 IMB-24-009 IMB-20-005 IMB-19-009 IMB-15-003 IMB-18-007 IMB-17-011 IMB-18-003 IMB-19-003 IMB-17-006 IMB-20-004 IMB-21-005 IMB-21-006 IMB-20-012 IMB-22-004 IMB-17-008 IMB-20-022 IMB-19-019 IMB-18-004 IMB-17-012 IMB-19-008 IMB-15-004 IMB-16-004 IMB-17-005 IMB-18-002 IMB-18-005 IMB-18-010 IMB-19-005 IMB-15-002 IMB-17-009 IMB-17-010 IMB-24-012 IMB-17-002 IMB-20-016 IMB-22-007 IMB-24-002 IMB-20-010 IMB-22-005 IMB-22-017 IMB-24-021 IMB-19-002 IMB-24-017 IMB-20-021 IMB-19-007 IMB-24-014 IMB-24-004 IMB-24-020 IMB-19-013 IMB-20-009 IMB-24-006 IMB-20-008 IMB-24-023 IMB-24-022 IMB-18-009 IMB-19-001 IMB-19-004 IMB-19-006 IMB-19-010 IMB-19-016 IMB-22-001 IMB-22-012 IMB-22-016 IMB-22-018 IMB-17-003 IMB-24-005 IMB-16-007 IMB-22-015 IMB-24-003 IMB-20-002 IMB-20-003 IMB-20-017 IMB-20-018 IMB-20-019 IMB-21-002 IMB-21-004 IMB-22-003 IMB-22-008 IMB-22-009 IMB-20-011 IMB-20-020; E85101LP: IMB-25-005 IMB-21-007 IMB-25-007 IMB-25-008 IMB-20-001 IMB-20-013 IMB-25-012 IMB-25-009 IMB-25-006 IMB-21-009 IMB-25-013 IMB-25-010 IMB-19-012 IMB-25-001 IMB-25-004 IMB-24-024 IMB-25-023 IMB-25-003
Recalling firm:
GE Medical Systems, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 3, 2026

IBA Proton Therapy System - PROTEUS 235

It was identified that eh Universal Beam Triggering Interface (UBTI) is disabled in the Therapy Safety System (TSS) configuration. In this condition, the TSS does not interrupt the beam delivery if the Healthy Signal from an external gating device is lost. This may lead to a risk of mistreatment when external gating devices are used.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98364
Lot/product code:
PROTEUS 235; UDI-DI: 05404013801138; Serial Numbers: SBF103 (JP), SBF124 (EU), SBF133 (US), SBF140 (EU)
Recalling firm:
Ion Beam Applications S.A.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 2, 2026

MICS3 Angled Sagittal Saw Attachment; Part Number: 210490

A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the cover to the Angled Saw Housing, may loosen during use and detach from the attachment.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98411
Lot/product code:
Part Number: 210490; UDI: (01)07613327523874(10)TU6563205RP; Lot numbers: ALL;
Recalling firm:
Howmedica Osteonics Corp.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 2, 2026

Brand Name: B. Braun Product Name: 21GA WINGED INF SET Model/Catalog Number: 7M2802 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection of air or fluids. Component: N/A

The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98380
Lot/product code:
Model/Catalog Number: 7M2802; Primary-DI 4046964787102, Unit of Use- DI 4046964349904; Lot 0062003864, Exp 30APR2032; Lot 0062004133, Exp 30JUN2032; Lot 0062006454, Exp 31JUL2032; Lot 0062028929, Exp 31AUG2032; Lot 0062037141, Exp 30SEP2032, Lot 0062037691, Exp 30SEP2032.
Recalling firm:
B Braun Medical Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 2, 2026

Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection of air or fluids. Component: N/A

The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98380
Lot/product code:
Model/Catalog Number: 7A3842; Primary-DI 4046964338434; Unit of Use- DI 4046964338410; Lot 0062004706, Exp 31MAR2032; Lot 0062005799, Exp 30JUN2032; Lot 0062006415, Exp 31MAR2032; Lot 0062006416, Exp 31MAR2032; Lot 0062023397, Exp 30JUN2032; Lot 0062024887, Exp 31JUL2032
Recalling firm:
B Braun Medical Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 2, 2026

Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Winged INF Model/Catalog Number: 7B3050 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection of air or fluids. Component: N/A

The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98380
Lot/product code:
Model/Catalog Number: 7B3050; Primary-DI 4046964341298, Unit of Use- DI 4046964341274; Lot 0062006430, Exp 30APR2032; Lot 0062006470, Exp 30JUN2032; Lot 0062006471, Exp 31MAY2032; Lot 0062014964, Exp 31JUL2032; Lot 0062014965, Exp 31JUL2032; Lot 0062014966, Exp 30SEP2032; Lot 0062027579, Exp 31AUG2032.
Recalling firm:
B Braun Medical Inc
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled February 2, 2026

Pro Numb Tattoo Numbing Spray, For Sensitive Skin, 4% Lidocaine, [1FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907, NDC 83389-112-11

CGMP deviations

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0303-2026
Lot/product code:
Lot Number J15
Recalling firm:
Pro Numb Tattoo Numbing Spray LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled February 2, 2026

Pro Numb Tattoo Numbing Spray, 5% Lidocaine, [1 FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907, NDC 83389-111-11

CGMP deviations

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0302-2026
Lot/product code:
Lot Numbers J01 through J14, J55 through J69
Recalling firm:
Pro Numb Tattoo Numbing Spray LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 1, 2026

On-X Mitral Heart Valve with Conform-X Sewing Ring, Model: ONXMC-25/33

Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release specifications.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98548
Lot/product code:
UDI-DI: 00851788001303. Serial Numbers: A2013401, A2013402, A2013403, A2013404, A2013405, A2013407, A2013408, A2013409, A2013410, A2013411. Expiration: 2031Dec17
Recalling firm:
On-X Life Technologies, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 30, 2026

Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit: 1) OPEN HEART, Model Number: DYNJ902487A; 2) CARDIAC PROCEDURE, Model Number: DYNJ908126; 3) CARDIO CONGENITO, Model Number: DYNJ910851

The instructions for use (IFUs) on specified Cardinal Health Chest Drainage Units (CDUs) and accessories have been updated to clarify the intended target patient population as adults, 18 years and older.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98437
Lot/product code:
1) DYNJ902487A, UDI-DI: 10193489496635(each), 40193489496636(case), Lot Number: 22KMG297; 2) DYNJ902487A, UDI-DI: 10193489496635(each), 40193489496636(case), Lot Number: 22FMA481; 3) DYNJ902487A, UDI-DI: 10193489496635(each), 40193489496636(case), Lot Number: 21IMG797; 4) DYNJ902487A, UDI-DI: 10193489496635(each), 40193489496636(case), Lot Number: 21HMG569; 5) DYNJ902487A, UDI-DI: 10193489496635(each), 40193489496636(case), Lot Number: 21HMB801; 6) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 26ABL637; 7) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 25JBN467M; 8) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 25JBN467; 9) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 25JBG183; 10) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 25HBF488; 11) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 25GBK350; 12) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 25FBO822; 13) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 25EBT976; 14) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 25EBP602; 15) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 25EBP589; 16) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 25EBP588; 17) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 25EBP587; 18) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 25EBP586; 19) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 25DBB810; 20) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 25ABA001; 21) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 24HBM020; 22) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 24GBC436; 23) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 24FBS256; 24) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 24BBP532; 25) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 24BBA256; 26) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 24ABN040; 27) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 23JBP214; 28) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 23JBJ077; 29) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 23IBQ646; 30) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 23HBU475; 31) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 23GBE710; 32) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 23GBE709; 33) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 23FBF593; 34) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 23DBJ852; 35) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 23DBC954; 36) DYNJ908126, UDI-DI: 10193489980110(each), 40193489980111(case), Lot Number: 22KBO714; 37) DYNJ910851, UDI-DI: 10198459155895(each), 40198459155896(case), Lot Number: 25IBK435; 38) DYNJ910851, UDI-DI: 10198459155895(each), 40198459155896(case), Lot Number: 25HBT069; 39) DYNJ910851, UDI-DI: 10198459155895(each), 40198459155896(case), Lot Number: 25HBO806; 40) DYNJ910851, UDI-DI: 10198459155895(each), 40198459155896(case), Lot Number: 25HBH137; 41) DYNJ910851, UDI-DI: 10198459155895(each), 40198459155896(case), Lot Number: 25GBA989; 42) DYNJ910851, UDI-DI: 10198459155895(each), 40198459155896(case), Lot Number: 24LBJ019
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 30, 2026

Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 5826659-027, 5826659-029, 5826659-032, 5826659-033, 5826659-028, 5826659-034, 5826659-030, 5826659-019, 5826659-022, 5826659-026, 5826659-023, 5826659-031, 5826659-025, 5826659-002, 5826659-021, 5826659-037, 5826659-014, 5826659-016, 5826659-013

There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98428
Lot/product code:
UDI Numbers: (01)00840682145794(10)70P004105825832001 (01)00840682145794(10)70P1015825832001 (01)00840682145794(10)70P1025825832001 (01)00840682145794(10)70P004105825832001 (01)00840682145794(10)70P1015825832001 (01)00840682145794(10)70P1015825832001 (01)00840682145794(10)70P1015825832001 (01)00840682145794(10)70P1015825832001 (01)00840682145794(10)70P1025825832001 (01)00840682145794(10)70P004105825832001 (01)00840682145794(10)70P1015825832001 (01)00840682145794(10)70P1025825832001 (01)00840682145794(10)70P1025825832001 (01)00840682145794(10)70P1025825832001 (01)00840682145794(10)70P1025825832001 (01)00840682145794(10)70P1035825832001 (01)00840682145794(10)70P1035825832001 (01)00840682145794(10)70P004105825832001 (01)00840682145794(10)70P004105825832001 (01)00840682145794(10)70P004105825832001 (01)00840682145794(10)70P004105825832001 (01)00840682145794(10)70P1035825832001 (01)00840682145794(10)70P004105825832001 (01)00840682145794(10)70P1035825832001 (01)00840682145794(10)70P1035825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P15825832001 (01)00840682145794(10)70P1035825832001 (01)00840682145794(10)70P1035825832001 (01)00840682145794(10)70P1045825832001 (01)00840682145794(10)70P1045825832001 (01)00840682145794(10)70P004105825832001 (01)00840682145794(10)70P0115825832001 (01)00840682145794(10)70P0115825832001 (01)00840682145794(10)70P0115825832001 (01)00840682145794(10)70P0115825832001 (01)00840682145794(10)70P0115825832001 (01)00840682145794(10)70P0115825832001 (01)00840682145794(10)70P0115825832001 (01)00840682145794(10)70P1015825832001 (01)00840682145794(10)70P1015825832001 (01)00840682145794(10)70P1045825832001 (01)00840682145794(10)70P1025825832001 (01)00840682145794(10)70P1025825832001 (01)00840682145794(10)70P1025825832001 (01)00840682145794(10)70P1025825832001 (01)00840682145794(10)70P1015825832001 (01)00840682145794(10)70P1025825832001 (01)00840682145794(10)70P1025825832001 (01)00840682145794(10)70P1025825832001 (01)00840682145794(10)70P1025825832001 (01)00840682145794(10)70P00445825832001 (01)00840682145794(10)70P00445825832001 (01)00840682145794(10)70P1025825832001 (01)00840682145794(10)70P1015825832001 (01)00840682145794(10)70P1025825832001 (01)00840682145794(10)70P00475825832001 (01)00840682145794(10)70P1015825832001 (01)00840682145794(10)70P00475825832001 (01)00840682145794(10)70P00475825832001 (01)00840682145794(10)70P1015825832001 (01)00840682145794(10)70P00475825832001 (01)00840682145794(10)70P00445825… (truncated, 61779 characters total — see the official FDA record for the full value)
Recalling firm:
GE Medical Systems, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 30, 2026

Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-406, 2100169-001, 2088026-985, 2088026-971, 2088026-614, 2088026-713, 2088026-994, 2100491-006, 2088026-723, 2088026-308, 2104867-044, 2100491-012, 2088026-962, 2088026-969, 2102676-001, 2088026-936, 2088026-960, K1220JWED, 2088026-806, 2088026-506, 2088026-026, 2088026-970, 2088026-943, 2088026-990, 2088026-940, 2088026-959, 2088026-967, 2088026-989, 2104867-045, 2088026-993, 2088026-306, 2102675-010, 2088026-948, 2088026-957, 2088026-973, 2088026-946, 2088026-715, 2088026-906

There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98428
Lot/product code:
UDI Numbers: (01)00840682103800(10)6.0SP42094097001D (01)00840682103800(10)6.0SP7.12094097001H (01)00840682103800(10)60P102.2094097001H (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)6.0SP62094097001D (01)00840682103800(10)6.0SP72094097001D (01)00840682103800(10)6.0SP72094097001D (01)00840682103800(10)6.0SP72094097001D (01)00840682103800(10)60P10412094097001 (01)00840682103800(10)60P10412094097001 (01)00840682103800(10)6.0SP5.0.12094097001D (01)00840682103800(10)6.0SP7.12094097001E (01)00840682103800(10)6.0SP7.12094097001E (01)00840682103800(10)6.0SP3.12094097001D (01)00840682103800(10)6.0SP3.12094097001D (01)00840682103800(10)6.0SP3.12094097001D (01)00840682103800(10)6.0SP3.12094097001D (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)6.0SP5.0.1.12094097001D (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)6.0SP5.0.12094097001D (01)00840682103800(10)6.0SP5.0.1.12094097001D (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)6.0SP5.0.12094097001D (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)6.0SP7.12094097001E (01)00840682103800(10)6.0SP7.12094097001E (01)00840682103800(10)6.0SP7.12094097001E (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)6.0SP5.0.12094097001D (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)6.0SP7.12094097001E (01)00840682103800(10)6.0SP7.12094097001E (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60SP90182094097001H (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)6.0SP42094097001D (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)6.0SP7.12094097001E (01)00840682103800(10)6.0SP3.12094097001D (01)00840682103800(10)6.0SP7.12094097001H (01)00840682103800(10)6.0SP7.12094097001H (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)6.0SP7.12094097001E (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)60P90111.2094097001H (01)00840682103800(10)60P90111.2094097001H (01)00840682103800(10)60P90111.2094097001H (01)00840682103800(10)6.0SP3.12094097001D (01)00840682103800(10)6.0SP7.12094097001E (01)00840682103800(10)6.0SP7.12094097001E (01)00840682103800(10)6.0SP7.12094097001E (01)00840682103800(10)6.0SP7.12094097001E (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)6.0SP5.0.32094097001D (01)00840682103800(10)60P90111.2094097001H (01)00840682103800(10)60P90111.2094097001H (01)00840682103800(10)60P90111.2094097001H (01)00840682103800(10)6.0SP5.0.32094097001D (01)00840682103800(10)6.0SP4.0.22094097001D (01)00840682103800(10)6.0SP7.12094097001E (01)00840682103800(10)6.0SP7.12094097001E (01)00840682103800(10)60SP90182094097001H (01)00840682103800(10)6.0SP9012094097001F (01)00840682103800(10)60SP90182094097001H (01)00840682103800(10)60P102.2094097001H (01)00840682103800(10)60P102.2094097001H (01)00840682103800(10)60P102.2094097001H (01)00840682103800(10)6.0SP5.0.32094097001D (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60SP90172094097001H (01)00840682103800(10)60SP90172094097001H (01)00840682103800(10)6.0SP7.12094097001E (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)6.0SP42094097001D (01)00840682103800(10)60P10412094097001 (01)00840682103800(10)6.0SP7.12094097001H (01)00840682103800(10)60SP5.0.42094097001D (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)60P901122094097001 (01)00840682103800(10)6.0SP62094097001D (01)00840682103800(10)6.0SP4.0.22094097001D (01)00840682103800(10)6.0SP4.0.220… (truncated, 32928 characters total — see the official FDA record for the full value)
Recalling firm:
GE Medical Systems, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 30, 2026

Tandem pumps are battery-operated infusion pumps capable of both basal and bolus delivery of insulin. The pumps utilize a motor-driven mechanism to deliver insulin from within a disposable cartridge, through an infusion set, into a patient s subcutaneous tissue. As with current insulin infusion pumps on the U.S. market, the desired timing and quantity of the insulin delivery is programmed by the user (i.e., the patient).

The Czech language user guide contained multiple translation errors. The most significant error was that it incorrectly instructs users to verify that the infusion set is connected to the body, when it should instead direct users to confirm that the infusion set is not connected to the body. Following this instruction could result in unintended insulin delivery, potentially leading to a hypoglycemic event.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98478
Lot/product code:
Version 7.8.1/ UDI: (01)008500066132625
Recalling firm:
Tandem Diabetes Care, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 30, 2026

Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-026, 2088026-115, 2088026-043, K2042VJED, 2088026-132, 2088026-003, 2088026-110, 2089629-003, 2066908-136, 2066908-150

There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98428
Lot/product code:
Product ID Numbers: 4446-2-Centricity Universal Viewer-00558643 100256-3-Centricity Universal Viewer-00558700 101044-1-Centricity Universal Viewer-00558694 13240-2-Centricity Universal Viewer-00558103 4441-1-Centricity Universal Viewer-00558677 4578-1-Centricity Universal Viewer-00558340 10831-2-Centricity Universal Viewer-00558682 656341-Centricity Universal Viewer-01431499 50567-Centricity Universal Viewer-02176369 2690973-Centricity Universal Viewer-01454622 EG1526-Centricity Universal Viewer-00158976 A91901-Centricity Universal Viewer-00044549 M3488569-Centricity Universal Viewer-00071707 25540620 - HC4105-Centricity Universal Viewer-00001393 416005-Centricity Universal Viewer-00260808 1868708X - 556162-Centricity Universal Viewer-00157857 HKOB01-Centricity Universal Viewer-01282268 BMH-Centricity Universal Viewer-01820534 JIPMER-Centricity Universal Viewer-01820555 4347967-Centricity Universal Viewer-01474540 651342-Centricity Universal Viewer-01365218 651342-Centricity Universal Viewer-01365213 A3431341-Centricity Universal Viewer-00545677 473265-Centricity Universal Viewer-01442014 JP-131575-Centricity Universal Viewer-01275307 442900-Centricity Universal Viewer-01460668 577127-Centricity Universal Viewer-01444349 349551-Centricity Universal Viewer-02350518 PL3277-Centricity Universal Viewer-00038831 RU3866-Centricity Universal Viewer-01445731 RU8945-Centricity Universal Viewer-01445740 RU2580-Centricity Universal Viewer-01445743 1354732-Centricity Universal Viewer-01273292 RU3453-Centricity Universal Viewer-01273249 SA2160-Centricity Universal Viewer-00111827 SA1208-Centricity Universal Viewer-00066587 882983-Centricity Universal Viewer-02277629 ZA2533-Centricity Universal Viewer-00116577
Recalling firm:
GE Medical Systems, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 30, 2026

HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product Number: VSLBASE03P / VITALSYNCSW03 Model / UDI-DI codes: Vital Sync 3.3.1 / 10884521844933 Vital Sync 3.4.0 / 10884521844940 Vital Sync 3.4.1 / 10884521847569 (OUS Only) Vital Sync 3.4.2 / 10884521856127 Product Number: VSLBASE04P / VITALSYNCSW04 Model / UDI-DI codes: Vital Sync 4.0.0 / 10884521849358 Vital Sync 4.0.2 / 10884521856134 The Vital Sync" Informatics Manager is software that is intended to route and store medical device data and device diagnostic information from supported devices to the Virtual Patient Monitoring Platform, 3rd Party Annunciation Systems, Electronic Medical Record (EMR) and Clinical Information System (CIS).

Due to complaints and investigations stating that alarms from the primary patient bedside monitor was not alarming/being transmitted and received on the remote patient monitoring system.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98407
Lot/product code:
HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: CFN: VSLBASE03P / VITALSYNCSW03 UDI-DI (GTIN); 10884521844933 Serial Number: Vital Sync 3.3.1 CFN: VSLBASE03P / VITALSYNCSW03 UDI-DI (GTIN): 10884521844940 Serial Number: Vital Sync 3.4.0 CFN: VSLBASE03P / VITALSYNCSW03 (OUS only) UDI-DI (GTIN): 10884521847569 Serial Number: Vital Sync 3.4.1 CFN: VSLBASE03P / VITALSYNCSW03 UDI-DI (GTIN): 10884521856127 Serial Number: Vital Sync 3.4.2 CFN: VSLBASE04P / VITALSYNCSW04 UDI-DI (GTIN): 10884521849358 Serial Number: Vital Sync 4.0.1 CFN: VSLBASE04P / VITALSYNCSW04 UDI-DI (GTIN): 10884521856134 Serial Number: Vital Sync 4.0.2
Recalling firm:
Covidien LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 30, 2026

MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61

Three software defects (Pump Error 53, BG check, and Critical Pump Error (Open Book Image)) that occurred as a result of software updates (versions 6.60, 6.61, and 6.62), which could result in a risk of hypoglycemia or hyperglycemia due to inaccuracies in insulin delivery (either under-delivery, over-delivery, or cessation of delivery).

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98444
Lot/product code:
MiniMed 780G Model Number: MMT-1884 UDI-DI code: 763000414344 Serial Numbers: NG2445689H NG2445778H NG2455039H NG2461527H NG2461608H NG2471389H NG2471573H NG2472820H NG2473989H NG2480622H NG2481237H NG2488091H NG2489139H NG2489358H NG2493893H NG2494899H NG2496212H NG2496474H NG2497261H NG2499391H NG2499496H NG2500475H NG2500548H NG2501835H NG2502145H NG2502898H NG2507769H NG2507907H NG2508301H NG2508631H NG2508977H NG2511996H NG2513292H NG2521020H NG2522070H NG2523184H NG2530419H NG2531373H NG2531462H NG2531531H NG2532792H NG2533855H NG2535235H NG2535576H NG2537531H NG2538456H NG2540108H NG2541102H NG2541837H NG2543029H NG2544725H NG2548997H NG2550437H NG2570180H NG2570258H NG2570863H NG2576778H NG2579113H NG2579956H NG2580323H NG2580479H NG2583059H NG2583537H NG2586717H NG2589082H NG2590426H NG2603812H NG2603854H NG2604027H NG2611960H NG2612797H NG2614177H NG2617670H NG2617983H NG2629660H NG2635544H NG2636572H NG2637401H NG2642169H NG2644227H NG2644567H NG2647406H NG2647913H NG2648318H NG2649298H NG2656257H NG2656473H NG2657321H NG2657360H NG2658332H NG2659390H NG2659574H NG2697897H NG2697936H NG2698209H NG2698900H NG2705266H NG2706152H NG2710968H NG2712109H NG2714386H NG2718094H NG2723617H NG2724376H NG2724445H NG2742517H NG2742729H NG2742925H NG2742927H NG2745927H NG2748918H NG2748985H NG2749113H NG2749121H NG2749143H NG2750007H NG2750299H NG2751081H NG2751191H NG2752539H NG2752574H NG2753164H NG2753234H NG2753931H NG2754038H NG2760759H NG2760871H NG2761027H NG2761050H NG2761095H NG2761117H NG2761226H NG2761771H NG2762312H NG2762332H NG2772977H NG2773133H NG2773170H NG2773198H NG2773224H NG2773698H NG2774482H NG2774486H NG2774628H NG2775088H NG2775593H NG2775790H NG2775796H NG2776055H NG2776076H NG2776843H NG2777281H NG2777366H NG2777406H NG2777964H NG2778250H NG2778518H NG2791067H NG2810990H NG2811465H NG2851127H NG2852041H NG2852121H NG2852167H NG2852226H NG2852237H NG2852293H NG2852641H NG2852707H NG2853049H NG2853185H NG2853369H NG2853574H NG2853980H NG2854083H NG2854095H NG2854218H NG2854266H NG2868862H NG2869169H NG2869564H NG2870219H NG2870848H NG2871392H NG2871868H NG2872358H NG2872379H NG2873197H NG2879290H NG2880034H NG2880037H NG2880061H NG2880324H NG2892508H NG2909952H NG2910456H NG2910488H NG2910742H NG2910995H NG2911113H NG2911329H NG2911785H NG2911915H NG2912050H NG2912065H NG2912195H NG2912304H NG2912412H NG2912423H NG2912530H NG2912600H NG2912625H NG2912670H NG2912798H NG2916905H NG2917028H NG2917060H NG2917238H NG2917352H NG2917461H NG2917748H NG2917757H NG2917849H NG2917881H NG2918087H NG2918234H NG2918273H NG2918540H NG2918762H NG2918951H NG2919128H NG2919210H NG2921713H NG2921759H NG2921764H NG2921912H NG2921960H NG2922097H NG2922157H NG2922350H NG2922515H NG2922615H NG2922632H NG2922633H NG2922990H NG2923035H NG2923056H NG2923120H NG2923140H NG2923262H NG2923459H NG2923582H NG2923832H NG2923995H NG2924042H NG2924152H NG2941414H NG2941570H NG2941614H NG2941619H NG2941809H NG2941839H NG2941875H NG2942123H NG2942193H NG2942249H NG2942367H NG2942645H NG2942782H NG2943281H NG2943510H NG2943529H NG2943592H NG2951199H NG2951224H NG2951253H NG2951586H NG2951675H NG2951690H NG2951706H NG2951750H NG2951859H NG2952135H NG2952255H NG2952320H NG2952397H NG2952463H NG2952485H NG2952507H NG2952650H NG2953269H NG2953290H NG2953392H NG2953536H NG2953801H NG2953875H NG2953954H NG2953997H NG2954054H NG2954081H NG2954200H NG2954202H NG2955586H NG2955592H NG2955666H NG2955753H NG2955756H NG2955850H NG2955927H NG2955990H NG2955994H NG2956003H NG2956028H NG2956052H NG2956167H NG2956214H NG2956245H NG2956375H NG2956416H NG2956504H NG2956533H NG2956561H NG2956567H NG2956660H NG2956711H NG2956824H NG2956934H NG2956979H NG2960027H NG2960318H NG2960498H NG2960556H NG2960899H NG2960914H NG2961016H NG2961049H NG2961106H NG2961108H NG2961114H NG2961187H NG2961287H NG2961320H NG2961354H NG2961405H NG2961445H NG2961655H NG2961682H NG2961761H NG2961771H NG2961782H NG2961813H NG2961906H NG2961958H NG2961965H NG2961968H NG2961995H NG2962012H NG2962032H NG2968147H NG2968281H NG2968308H NG2968340H NG2968491H NG2968492H NG2968499H NG2968805H NG2968842H NG2968986H NG2969067H NG2969111H NG2969152H NG2969273H NG2969277H NG2969388H NG2969415H NG2969441H NG2969468H NG2969542H NG2969582H NG2969745H NG2980849H NG2980857H NG2980875H NG2980916H NG2981068H NG2981268H NG2981313H NG2981419H NG2981696H NG2981774H NG2981975H NG2981985H NG2982089H NG2982172H NG2982232H NG2982281H NG2982538H NG2982662H NG2982763H NG2982864H NG2982878H NG2982896H NG2982986H NG2983018H NG3001336H NG3001600H NG3001820H NG3001831H NG3001921H NG3002022H NG3002026H NG3002037H NG3002060H NG3002155H NG3002250H NG3002265H NG3002371H NG3002388H NG3002553H NG3002580H NG3002594H NG3002602H NG3002608H NG3002641H NG3002652H NG3002681H NG3002708H NG3002710H NG3002734H NG3002762H NG3002772H NG3002782H NG3002909H NG3002911H NG3002929H NG3002958H NG3002962H NG3002996H NG3003022H NG3003051H NG3003153H NG3010488H NG3010602H NG3010604H NG3039386H NG3039702H NG3039783H NG303… (truncated, 298713 characters total — see the official FDA record for the full value)
Recalling firm:
Medtronic MiniMed, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 29, 2026

Brand Name: Paradise Ultrasound Renal Denervation System Product Name: Paradise Catheter Model/Catalog Number: PRDS-068-02 Product Description: Common name: Ablation catheter renal denervation

Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98365
Lot/product code:
Lot Code: Model No PRDS-068-02; UDI-DI 00810008950043; Lot Number: M4907
Recalling firm:
ReCor Medical Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 29, 2026

Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. The MAJ-1218 has been designed to be attached to the instrument channel port of compatible endoscopes to prevent leakage of body fluids.

Potential for rubber fragment detachment during use.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98240
Lot/product code:
Model/Catalog Number: MAJ-1218. UDI-DI: 14953170154291. All Lot Numbers. 20 units per box.
Recalling firm:
Olympus Corporation of the Americas
View official FDA record (opens in a new tab)