BIGNOPE
Ko-fi

Recalls affecting Arizona

Data last updated: September 9, 2026 at 1:18 PM UTC

16,936 recalls found
NewOld
High RiskLow Risk
AllClear

Just announced

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

Business Pill, Branch Manager for Men — dietary 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 Alive — Moringa 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. Braun — 0.9% 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 Value — Organic 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)
UnclassifiedUndeclaredAnnounced August 31, 2026

Lipofit — Lipofit 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

Kofinas — Garlic 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)
UnclassifiedAllergenMilkUndeclaredAnnounced August 31, 2026

Little Temptations — Chocolatey 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)
UnclassifiedBacteria/virusSalmonellaE. coliAnnounced August 29, 2026

Everything Sprouts — Robust 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

Martina — Mangoes

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 April 10, 2026

Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo EVD Catheter is a 3.3 mm diameter (10 Fr.), 35 cm long polyurethane catheter for diverting cerebrospinal fluid (CSF) from the ventricles of the brain through a series of drainage holes near the catheter's bullet shaped tip.

Not meeting quality requirements endotoxin result that did not meet the acceptance criteria.

ALL 50 STATES
▸Full report

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

Recall #:
98752
Lot/product code:
Product ID: 37.550.501. UDI-DI: 10381780530138. Lot Number: 45322.
Recalling firm:
Integra LifeSciences Corp. (NeuroSciences)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 10, 2026

Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: SPINAL BLOCK 22G QUINCKE 5S BU, Medline Kit SKU DYNJRA9026

Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

ALL 50 STATES
▸Full report

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

Recall #:
98837
Lot/product code:
Medline Kit SKU DYNJRA9026: UDI/DI 10884389285688 each, 40884389285689, case, Lot Numbers: 26BBD235, 26ABB534, 25DBT837, 25CBH118, 24FBT403, 24FBJ505.
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 10, 2026

Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL ANESTHESIA TRAY-LF, Medline Kit SKU DYNJRA0102A; 2) SPINAL TRAY-LF, Medline Kit SKU DYNJRA0143B; 3) SPINAL PREP TRAY-LF, Medline Kit SKU DYNJRA0205B; 4) SPINAL TRAY, Medline Kit SKU DYNJRA0255B; 5) SPINAL TRAY, Medline Kit SKU DYNJRA0320; 6) SPINAL TRAY, Medline Kit SKU DYNJRA0320A; 7) SPINAL BLOCK TRAY- LF, Medline Kit SKU DYNJRA0413C; 8) SPINAL TRAY, Medline Kit SKU DYNJRA0461D; 9) 25G SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA0945; 10) SPINAL TRAY, Medline Kit SKU DYNJRA1140B; 11) SPINAL TRAY, Medline Kit SKU DYNJRA1192; 12) SPINAL TRAY 25G, Medline Kit SKU DYNJRA1240; 13) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA1288; 14) SPINAL 25G WHITACRE, Medline Kit SKU DYNJRA1301; 15) SPINAL BLOCK TRAY WHITACRE 24G, Medline Kit SKU DYNJRA1304; 16) AHN SPINAL TRAY, Medline Kit SKU DYNJRA1376; 17) SPINAL TRAY, Medline Kit SKU DYNJRA1477A; 18) ADULT SPINAL KIT, Medline Kit SKU DYNJRA1538; 19) SPINAL TRAY, Medline Kit SKU DYNJRA1558A; 20) SPINAL TRAY, Medline Kit SKU DYNJRA1560A; 21) SPINAL TRAY, Medline Kit SKU DYNJRA1565; 22) SPINAL ANESTHESIA TRAY, Medline Kit SKU DYNJRA1577C; 23) SPINAL NEEDLE TRAY, Medline Kit SKU DYNJRA1584; 24) 25G WHITACRE SPINAL TRAY, Medline Kit SKU DYNJRA1740A; 25) SPINAL TRAY, Medline Kit SKU DYNJRA1744A; 26) SPINAL TRAY, Medline Kit SKU DYNJRA1750A; 27) SPINAL TRAY, Medline Kit SKU DYNJRA1784; 28) SPINAL TRAY, Medline Kit SKU DYNJRA1790; 29) SPINAL TRAY, Medline Kit SKU DYNJRA1796; 30) MSSC SPINAL TRAY, Medline Kit SKU DYNJRA1802B; 31) SPINAL TRAY, Medline Kit SKU DYNJRA1818; 32) SPINAL TRAY, Medline Kit SKU DYNJRA1839; 33) SPINAL TRAY, Medline Kit SKU DYNJRA1884; 34) SPINAL TRAY, Medline Kit SKU DYNJRA1884A; 35) 24G SPINAL KIT, Medline Kit SKU DYNJRA1889; 36) SPINAL TRAY, Medline Kit SKU DYNJRA1929; 37) SPINAL TRAY, Medline Kit SKU DYNJRA1969; 38) SPINAL TRAY, Medline Kit SKU DYNJRA1982; 39) SPINAL TRAY/PENCAN, Medline Kit SKU DYNJRA1983A; 40) SPINAL NEEDLE TRAY, Medline Kit SKU DYNJRA1987; 41) SPINAL TRAY - 3 ML CHLORAPREP, Medline Kit SKU DYNJRA2005; 42) SPINAL TRAY, Medline Kit SKU DYNJRA2023; 43) SPINAL TRAY, Medline Kit SKU DYNJRA2068A; 44) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2088; 45) 25G WHITACRE SPINAL TRAY, Medline Kit SKU DYNJRA2115; 46) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKU DYNJRA2117; 47) SPINAL TRAY, Medline Kit SKU DYNJRA2140; 48) SPINAL TRAY, Medline Kit SKU DYNJRA2153; 49) SPINAL BLOCK TRAY WHITACRE 24G, Medline Kit SKU DYNJRA2213; 50) SPINAL TRAY, Medline Kit SKU DYNJRA2225; 51) OR SPINAL BLOCK KIT, Medline Kit SKU DYNJRA2349; 52) SPINAL TRAY, Medline Kit SKU DYNJRA2360; 53) L&D SPINAL TRAY, Medline Kit SKU DYNJRA2371; 54) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2381; 55) SPINAL TRAY, Medline Kit SKU DYNJRA2432A; 56) OB SPINAL TRAY, Medline Kit SKU DYNJRA2532; 57) SPINAL TRAY, Medline Kit SKU DYNJRA2534; 58) SPINAL TRAY, Medline Kit SKU DYNJRA2556; 59) SPINAL TRAY, Medline Kit SKU DYNJRA2566A; 60) SPINAL TRAY BRAUN, Medline Kit SKU DYNJRA2575; 61) SPINAL TRAY, Medline Kit SKU DYNJRA2592; 62) SPINAL TRAY, Medline Kit SKU DYNJRA2597; 63) SPINAL BLOCK, Medline Kit SKU DYNJRA2605; 64) SPINAL TRAY, Medline Kit SKU DYNJRA2606; 65) SPINAL TRAY, Medline Kit SKU DYNJRA2607; 66) SPINAL TRAY, Medline Kit SKU DYNJRA2607A; 67) SPINAL TRAY, Medline Kit SKU DYNJRA2611; 68) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2613; 69) SPINAL TRAY, Medline Kit SKU DYNJRA2618A; 70) SPINAL TRAY, Medline Kit SKU DYNJRA2634; 71) SPINAL TRAY, Medline Kit SKU DYNJRA2638; 72) SPINAL TRAY, Medline Kit SKU DYNJRA2639; 73) JOI SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2641; 74) SPINAL TRAY, Medline Kit SKU DYNJRA2653; 75) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKU DYNJRA2669; 76) SPINAL TRAY, Medline Kit SKU DYNJRA2670; 77) SPINAL BLOCK TRAY 18G INTRO, Medline Kit SKU DYNJRA2672; 78) SPINAL TRAY 24G, Medline Kit

Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

ALL 50 STATES
▸Full report

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

Recall #:
98837
Lot/product code:
Medline Kit SKU DYNJRA0102A: UDI/DI 10884389459003 each, 40884389459004 case, Lot Number 26ABG838; Medline Kit SKU DYNJRA0102A: UDI/DI 10884389459003 each, 40884389459004 case, Lot Number 25JBR222; Medline Kit SKU DYNJRA0102A: UDI/DI 10884389459003 each, 40884389459004 case, Lot Number 25IBJ307; Medline Kit SKU DYNJRA0102A: UDI/DI 10884389459003 each, 40884389459004 case, Lot Number 25EBR346; Medline Kit SKU DYNJRA0102A: UDI/DI 10884389459003 each, 40884389459004 case, Lot Number 24LDB145; Medline Kit SKU DYNJRA0102A: UDI/DI 10884389459003 each, 40884389459004 case, Lot Number 24FDB896; Medline Kit SKU DYNJRA0143B: UDI/DI 10195327125820 each, 40195327125821 case, Lot Number 24ABQ670; Medline Kit SKU DYNJRA0205B: UDI/DI 10195327472344 each, 40195327472345 case, Lot Number 24KMD212; Medline Kit SKU DYNJRA0255B: UDI/DI 10195327282042 each, 40195327282043 case, Lot Number 26CMG585; Medline Kit SKU DYNJRA0255B: UDI/DI 10195327282042 each, 40195327282043 case, Lot Number 26BMK211; Medline Kit SKU DYNJRA0255B: UDI/DI 10195327282042 each, 40195327282043 case, Lot Number 25JMC385; Medline Kit SKU DYNJRA0255B: UDI/DI 10195327282042 each, 40195327282043 case, Lot Number 25IMB105; Medline Kit SKU DYNJRA0255B: UDI/DI 10195327282042 each, 40195327282043 case, Lot Number 25EMC687; Medline Kit SKU DYNJRA0255B: UDI/DI 10195327282042 each, 40195327282043 case, Lot Number 24HMD675; Medline Kit SKU DYNJRA0255B: UDI/DI 10195327282042 each, 40195327282043 case, Lot Number 24HMB249; Medline Kit SKU DYNJRA0255B: UDI/DI 10195327282042 each, 40195327282043 case, Lot Number 24GMH436; Medline Kit SKU DYNJRA0320: UDI/DI 10884389656778 each, 40884389656779 case, Lot Number 24EDB314; Medline Kit SKU DYNJRA0320: UDI/DI 10884389656778 each, 40884389656779 case, Lot Number 24BDA550; Medline Kit SKU DYNJRA0320A: UDI/DI 10198459027796 each, 40198459027797 case, Lot Number 26ABJ309; Medline Kit SKU DYNJRA0320A: UDI/DI 10198459027796 each, 40198459027797 case, Lot Number 25HBT750; Medline Kit SKU DYNJRA0320A: UDI/DI 10198459027796 each, 40198459027797 case, Lot Number 25GBW261; Medline Kit SKU DYNJRA0320A: UDI/DI 10198459027796 each, 40198459027797 case, Lot Number 25FBP025; Medline Kit SKU DYNJRA0413C: UDI/DI 10195327253363 each, 40195327253364 case, Lot Number 26AMK323; Medline Kit SKU DYNJRA0413C: UDI/DI 10195327253363 each, 40195327253364 case, Lot Number 25HMB655; Medline Kit SKU DYNJRA0413C: UDI/DI 10195327253363 each, 40195327253364 case, Lot Number 25FMF763; Medline Kit SKU DYNJRA0413C: UDI/DI 10195327253363 each, 40195327253364 case, Lot Number 24KMF380; Medline Kit SKU DYNJRA0413C: UDI/DI 10195327253363 each, 40195327253364 case, Lot Number 24KMA760; Medline Kit SKU DYNJRA0413C: UDI/DI 10195327253363 each, 40195327253364 case, Lot Number 23IBH412; Medline Kit SKU DYNJRA0461D: UDI/DI 10195327120689 each, 40195327120680 case, Lot Number 24KME483; Medline Kit SKU DYNJRA0461D: UDI/DI 10195327120689 each, 40195327120680 case, Lot Number 23KMD757; Medline Kit SKU DYNJRA0945: UDI/DI 10889942598267 each, 40889942598268 case, Lot Number 26BBP431; Medline Kit SKU DYNJRA0945: UDI/DI 10889942598267 each, 40889942598268 case, Lot Number 25KBN750; Medline Kit SKU DYNJRA0945: UDI/DI 10889942598267 each, 40889942598268 case, Lot Number 25IBK141; Medline Kit SKU DYNJRA0945: UDI/DI 10889942598267 each, 40889942598268 case, Lot Number 25EBG343; Medline Kit SKU DYNJRA0945: UDI/DI 10889942598267 each, 40889942598268 case, Lot Number 25ADA288; Medline Kit SKU DYNJRA0945: UDI/DI 10889942598267 each, 40889942598268 case, Lot Number 24FDA636; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 26BMI341; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 25LMF246; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 25JMA359; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 25GMB242; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 25DMI678; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 24JMA139; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 24BME491; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 23KMB687; Medline Kit SKU DYNJRA1140B: UDI/DI 10193489432015 each, 40193489432016 case, Lot Number 23HMD531; Medline Kit SKU DYNJRA1192: UDI/DI 10888277762947 each, 40888277762948 case, Lot Number 24JDA083; Medline Kit SKU DYNJRA1192: UDI/DI 10888277762947 each, 40888277762948 case, Lot Number 24FDA375; Medline Kit SKU DYNJRA1192: UDI/DI 10888277762947 each, 40888277762948 case, Lot Number 24CDA048; Medline Kit SKU DYNJRA1192: UDI/DI 10888277762947 each, 40888277762948 case, Lot Number 23KDC201; Medline Kit SKU DYNJRA1192: UDI/DI 10888277762947 each, 408882… (truncated, 49024 characters total — see the official FDA record for the full value)
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 10, 2026

Daig Livewire Steerable, Product Number 401652; REPROCESSED ELECTROPHYSIOLOGY CATHETER

Incomplete seals on sterile product

ALL 50 STATES
▸Full report

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

Recall #:
98708
Lot/product code:
UDI 00885825006983, Lot Numbers: 3430230, 4648604, 4945422, 4999751, 5044134, 5059493, 4454505, 4882788, 4950218, 4999755, 5044135, 5086419, 4454517, 4945388, 4993562, 5044132, 5044136, 5086420, 4648603, 4945405, 4993565, 5044133, 5044137.
Recalling firm:
Stryker Sustainability Solutions
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 9, 2026

Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube Sets are intended to be used with the FluidSmart Fluid Management System, which is intended for irrigation and fluid warming in laparoscopic procedures, and distention, fluid warming, and volume/deficit measurements in endoscopic procedures within gynecology, urology, and orthopedic disciplines.

Due to nonconforming products being inadvertently distributed.

ALL 50 STATES
▸Full report

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

Recall #:
98696
Lot/product code:
Catalog Number: LL0006 UDI-DI code: 00860936000365 Lot Number: B000576601
Recalling firm:
Stryker Corporation
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled April 9, 2026

Omega-3-Acid, Ethyl Esters, Capsules, USP, 1 gram, 50 capsules (5 x 10 unit dose blister cards) per carton, Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46288. NDC: 0904-7495-06

Failed Capsule Specifications: not meeting quality requirements results obtained during routine stability testing for Loss on Drying of Capsule Shells.

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-0493-2026
Lot/product code:
Lot#: Lot N02406, Exp 10/31/2026; Lot N02845, Exp 12/31/2026
Recalling firm:
The Harvard Drug Group LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled April 8, 2026

Revitaderm Wound Care, First Aid Antiseptic Gel, Benzalkonium Chloride 0.1%) packaged as (a) 1.0 Fl OZ (16 mL) bottle, long pointy cap, NDC 63347-120-02; (b) 3.0 Fl OZ (85 g) tube, with short twist cap, NDC 63347-120-01; Manufactured By: Blaine Labs, Inc. 11037 Lockport Place, Santa Fe Springs, CA 90670,

CGMP Deviations; product manufactured in the same facility under the same conditions as the product found to be contaminated

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-0699-2026
Lot/product code:
Lots: (a) 1 oz - BL3435, Exp 11/06/26; BL3525, Exp 08/07/27. (b) 3 oz- Lots # BL3435, 11/06/26 & BL3525, 08/07/27
Recalling firm:
Blaine Labs Inc
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled April 8, 2026

TERPENICOL Antifungal Cream (Undecylenic Acid 13%), 1.0 oz (28 g) bottles, Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Sante Fe Springs, CA 90670, NDC 63347-601-01.

CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry

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-0695-2026
Lot/product code:
Lots BL3431R, Exp Date 10/13/26 & BL3528, Exp Date 08/30/2027.
Recalling firm:
Blaine Labs Inc
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled April 8, 2026

Fungal Fusion ERADICATION Solution, Antifungal & Antimicrobial Kit. Contains, 1x2 oz bottle Fungal Fusion Antifungal (Miconazole Nitrate) Cream, 1x2oz bottle Fungal Fusion Antifungal Solution (25% Undecylenic Acid) and 1x1oz bottle of Fungal Fusion Eradication Antimicrobial Show Spray (isopropyl Alcohol, D-Limonene, Undecylenic Acid). Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Santa Fe Springs, CA 90670, Manufactured for Doctor's Inc

CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry

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-0698-2026
Lot/product code:
Lot BL3572, Exp 04/16/2028
Recalling firm:
Blaine Labs Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled April 8, 2026

Revitaderm Wound Care Gel, Benzalkonium Chloride 0.1%, packaged in 1.0 FL OZ (37 mL) bottle, shorter twist cap, Manufactured By: Blaine Labs, Inc. 11037 Lockport Place Santa Fe Springs, CA 90670, NDC 63347-120-02.

Microbial contamination of Non-Sterile Product: samples identified the presence of Lysinibacillus fusiformis and other Bacillus spp

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0692-2026
Lot/product code:
Lot#: BL3608, Exp. 07/01/28.
Recalling firm:
Blaine Labs Inc
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled April 8, 2026

TRIPENICOL S Antifungal Solution (Undecylenic Acid 25%), 1.25 FL OZ (37.5 mL) bottle, Manufactured For: Trifluent Pharma, LLC, San Antonio, TX 78213, NDC 73352-550-01.

CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry

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-0694-2026
Lot/product code:
Lot #BL3411R, Exp 6/8/2027
Recalling firm:
Blaine Labs Inc
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled April 8, 2026

TERPENICOL Antifungal Solution, (Undecylenic (10-Undecenoic) acid 25%), 1.0 Fl Oz (29.6 mL), Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Santa Fe Springs, CA 90670. NDC 63347-600-01

CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry

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-0697-2026
Lot/product code:
Lots BL3411R, Exp Date 06/08/2027, BL3468, Exp Date 03/07/2027, & BL3535, Exp Date 09/25/2027.
Recalling firm:
Blaine Labs Inc
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled April 8, 2026

Desmopressin Nasal Spray, USP, 10 mcg/0.1 mL, 5 mL bottle (50 doses), Rx only, Mfg by: Apotek inc., Toronto, Ontario, Canada, M9L 1T9, Mfg for: Apotek Corp., Weston, FL 33326, NDC 60505-0815-0

Defective container: defect in a batch of bottle caps, specifically involving dislodged or missing cap liners.

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-0510-2026
Lot/product code:
Lot #: VM4231, Exp 06/30/2027
Recalling firm:
Apotex Corp.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled April 8, 2026

TRIFLUENT PHARMA TRIDERGEL Wound Care Gel, (Benzalkonium Chloride 0.1%), 1.0 fl oz, (29.6 mL) bottle with long pointy cap, Manufactured for: Trifluent Pharma, LLC. San Antonio, TX 78213. NDC 73352-520-01.

CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated

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-0693-2026
Lot/product code:
Lot #: BL3435, Exp. 11/06/26
Recalling firm:
Blaine Labs Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 8, 2026

3DIMENSIONS MAMMOGRAPHY SYSTEM; Model Numbers: 3DM-SYS-INTL2D, 3DM-SYS-INTL2D-MOB, 3DM-SYS-INTL2D-NS, 3DM-SYS-INTL3D, 3DM-SYS-INTL3D-MOB, 3DM-SYS-INTL3D-NS, 3DM-SYS-STD, 3DM-SYS-STD-MOB, 3DM-SYS-STD-NS.

Complaints have been received of systems developing loose, missing, or broken internal bolts over time.

ALL 50 STATES
▸Full report

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

Recall #:
98566
Lot/product code:
"[Model No.; UDI]: [3DM-SYS-INTL2D;15420045510609], [3DM-SYS-INTL2D-MOB;15420045510593], [3DM-SYS-INTL2D-NS;15420045510586], [3DM-SYS-INTL3D;15420045510579], [3DM-SYS-INTL3D-MOB;15420045510562], [3DM-SYS-INTL3D-NS;15420045510555], [3DM-SYS-STD;15420045510524], [3DM-SYS-STD-MOB;15420045510531], [3DM-SYS-STD-NS;15420045510548]; All Serial No.
Recalling firm:
Hologic, Inc
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled April 8, 2026

vite20 Antifungal Cream, (10% Undecylenic Acid), 0.54 OZ (15 g) bottle, Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Sante Fe Springs, CA 90670, UPC 6 16728 00039 2.

CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry

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-0696-2026
Lot/product code:
Lot BL3462, Exp. 2/7/2027
Recalling firm:
Blaine Labs Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 8, 2026

Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application, loaded on the following devices: 1. PROG CT900A CLINICIAN TABLET US, Model Number CT900A; 2. PROG CT900B CLINICIAN TABLET EU -UK, Model Number CT900B; 3. PROG CT900C CLINICIAN TABLET UK, Model Number CT900C; 4. PROG CT900D CLINICIAN TABLET GLOBAL, Model Number CT900D; 5. PROG CT900E CLINICIAN TABLET GLBL SMSNG, Model Number CT900E; 6. PROG CT900F CLINICIAN TABLET GLBL SMSNG, Model Number CT900F; implanted programmable infusion pump

Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in consecutive order, from earliest to latest. However, in rare cases, the steps may be displayed out of order. If this occurs, the programmed Flex Infusion schedule will not be delivered at the intended time, if at all.

ALL 50 STATES
▸Full report

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

Recall #:
98750
Lot/product code:
Software application (app) version 1.x and 2.x, loaded on the following units: 1. Model Number CT900A, GTIN 00643169890923, Serial Numbers: NPL0004445; 2. Model Number CT900B, GTIN 00643169890947, Serial Numbers: NPL1000042, NPL1000045, NPL1000046, NPL1000048, NPL1000050, NPL1000051, NPL1000053, NPL1000054, NPL1000059, NPL1000060, NPL1000062, NPL1000065, NPL1000069, NPL1000070, NPL1000071, NPL1000072, NPL1000073, NPL1000074, NPL1000075, NPL1000077, NPL1000081, NPL1000082, NPL1000083, NPL1000085, NPL1000086, NPL1000087, NPL1000090, NPL1000091, NPL1000093, NPL1000094, NPL1000098, NPL1000117, NPL1000133, NPL1000135, NPL1000137, NPL1000138, NPL1000151, NPL1000159, NPL1000160, NPL1000164, NPL1000166, NPL1000167, NPL1000169, NPL1000173, NPL1000174, NPL1000179, NPL1000180, NPL1000183, NPL1000185, NPL1000186, NPL1000187, NPL1000188, NPL1000191, NPL1000192, NPL1000193, NPL1000194, NPL1000195, NPL1000196, NPL1000230, NPL1000235, NPL1000237, NPL1000242, NPL1000244, NPL1000245, NPL1000246, NPL1000248, NPL1000249, NPL1000252, NPL1000254, NPL1000257, NPL1000258, NPL1000281, NPL1000292, NPL1000297, NPL1000301, NPL1000303, NPL1000307, NPL1000321, NPL1000322, NPL1000323, NPL1000325, NPL1000326, NPL1000332, NPL1000334, NPL1000343, NPL1000361, NPL1000362, NPL1000363, NPL1000364, NPL1000365, NPL1000366, NPL1000367, NPL1000369, NPL1000370, NPL1000381, NPL1000483, NPL1000486, NPL1000487, NPL1000501, NPL1000502, NPL1000505, NPL1000506, NPL1000507, NPL1000509, NPL1000510, NPL1000512, NPL1000515, NPL1000516, NPL1000518, NPL1000519, NPL1000528, NPL1000529, NPL1000539, NPL1000540, NPL1000555, NPL1000556, NPL1000558, NPL1000560, NPL1000561, NPL1000562, NPL1000563, NPL1000564, NPL1000571, NPL1000573, NPL1000574, NPL1000575, NPL1000576, NPL1000577, NPL1000578, NPL1000580, NPL1000585, NPL1000592, NPL1000603, NPL1000606, NPL1000612, NPL1000627, NPL1000630, NPL1000631, NPL1000632, NPL1000634, NPL1000637, NPL1000641, NPL1000652, NPL1000653, NPL1001194, NPL1001195, NPL1001201, NPL1001204, NPL1001205, NPL1001206, NPL1001207, NPL1001208, NPL1001210, NPL1001211, NPL1001212, NPL1001216, NPL1001223, NPL1001224, NPL1001225, NPL1001226, NPL1001228, NPL1001229, NPL1001230, NPL1001231, NPL1001235, NPL1001236, NPL1001237, NPL1001238, NPL1001240, NPL1001241, NPL1001243, NPL1001244, NPL1001250, NPL1001251, NPL1001254, NPL1001259, NPL1001264, NPL1001265, NPL1001272, NPL1001273, NPL1001274, NPL1001277, NPL1001282, NPL1001283, NPL1001290, NPL1001291, NPL1001306, NPL1001307, NPL1001313, NPL1001314, NPL1001328, NPL1001330, NPL1001332, NPL1001333, NPL1001334, NPL1001336, NPL1001337, NPL1001339, NPL1001341, NPL1001345, NPL1001349, NPL1001350, NPL1001351, NPL1001353, NPL1001354, NPL1001360, NPL1001361, NPL1001362, NPL1001366, NPL1001367, NPL1001369, NPL1001372, NPL1001375, NPL1001380, NPL1001381, NPL1001385, NPL1001386, NPL1001389, NPL1001398, NPL1001407, NPL1001408, NPL1001410, NPL1001412, NPL1001419, NPL1001421, NPL1001423, NPL1001430, NPL1001431, NPL1001434, NPL1001435, NPL1001436, NPL1001439, NPL1001445, NPL1001449, NPL1001458, NPL1001461, NPL1001464, NPL1001465, NPL1001468, NPL1001482, NPL1001483, NPL1001486, NPL1001499, NPL1001500, NPL1001505, NPL1001507, NPL1001510, NPL1001512, NPL1001513, NPL1001514, NPL1001518, NPL1001520, NPL1001524, NPL1001526, NPL1001531, NPL1001532, NPL1001537, NPL1001539, NPL1001540, NPL1001541, NPL1001542, NPL1001544, NPL1001545, NPL1001546, NPL1001547, NPL1001549, NPL1001550, NPL1001678, NPL1001689, NPL1001694, NPL1001695, NPL1001697, NPL1001699, NPL1001700, NPL1001701, NPL1001702, NPL1001705, NPL1001707, NPL1001708, NPL1001709, NPL1001710, NPL1001711, NPL1001716, NPL1001717, NPL1001723, NPL1001724, NPL1001727, NPL1001728, NPL1001739, NPL1001740, NPL1001741, NPL1001742, NPL1001743, NPL1001744, NPL1001745, NPL1001748, NPL1001749, NPL1001750, NPL1001754, NPL1001755, NPL1001756, NPL1001757, NPL1001759, NPL1001760, NPL1001761, NPL1001763, NPL1001764, NPL1001765, NPL1001766, NPL1001767, NPL1001769, NPL1001770, NPL1001773, NPL1001777, NPL1001784, NPL1001787, NPL1001789, NPL1001792, NPL1001794, NPL1001795, NPL1001797, NPL1001798, NPL1001799, NPL1001800, NPL1001801, NPL1001803, NPL1001804, NPL1001805, NPL1001806, NPL1001811, NPL1001812, NPL1001815, NPL1001816, NPL1001817, NPL1001820, NPL1001823, NPL1001824, NPL1001825, NPL1001829, NPL1001830, NPL1001833, NPL1001841, NPL1001842, NPL1001843, NPL1001844, NPL1001847, NPL1001875, NPL1001876, NPL1001877, NPL1001879, NPL1001880, NPL1001881, NPL1001882, NPL1001884, NPL1001885, NPL1001886, NPL1001887, NPL1001888, NPL1001889, NPL1001891, NPL1001897, NPL1001899, NPL1001900, NPL1001901, NPL1001903, NPL1001904, NPL1001905, NPL1001937, NPL1001940, NPL1001946, NPL1001947, NPL1001948, NPL1001950, NPL1001955, NPL1001957, NPL1001959, NPL1001963, NPL1001966, NPL1001968, NPL1001969, NPL1001970, NPL1001971, NPL1001972, NPL1001973, NPL1001974, NPL1001975, NPL1001976, NPL1001977, NPL1001995, NPL1001996, NPL1002004, NPL1002007, NPL1002010, NPL1002016, NPL1002020, NPL1002021, NPL1002025, NPL1002034, NPL10… (truncated, 122673 characters total — see the official FDA record for the full value)
Recalling firm:
Medtronic Neuromodulation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 8, 2026

Swan-Ganz Pacing Catheter, Models: D200F7;

Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.

ALL 50 STATES
▸Full report

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

Recall #:
98603
Lot/product code:
Model-UDI-DI/Lot(Expiration): D200F7-00690103147315/66725358(7/2/2027)
Recalling firm:
Becton, Dickinson and Company
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 8, 2026

Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7, 831F75/831F75P, TS105F5, 774F75, 777F8, AIQSGF8;

Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.

ALL 50 STATES
▸Full report

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

Recall #:
98603
Lot/product code:
Model/UDI-DI/Lot(Expiration): 131F7P/00690103000412/65902900(8/1/2026), 65902901(8/3/2026), 65910728(8/2/2026), 65910729(7/29/2026),65910730(7/27/2026), 65910731(7/25/2026), 65910732(7/26/2026), 65910735(7/30/2026), 65910736(8/24/2026), 65910737(7/31/2026), 65916927(8/3/2026), 65916928(8/6/2026), 65916929(8/7/2026), 65916930(8/8/2026), 65916931(8/9/2026), 65916932(8/22/2026), 65916933(8/23/2026), 65944791(8/20/2026),65944792(8/21/2026), 65955857(9/9/2026), 65955858(9/17/2026), 65955859(9/26/2026), 65955860(9/27/2026), 65973739(9/5/2026), 65973740(9/6/2026), 65973741(9/7/2026), 65973742(9/10/2026), 65988571(9/28/2026), 65997478(9/16/2026), 65997479(9/17/2026), 65997481(9/19/2026), 65997482(9/20/2026), 66010504(9/10/2026), 66010505(9/11/2026), 66010506(9/12/2026), 66010507(9/13/2026), 66010508(9/14/2026), 66023074(9/30/2026), 66033088(10/5/2026), 66048930(10/9/2026), 66057629(10/6/2026), 66057630(10/8/2026), 66057944(10/15/2026), 66057945(10/17/2026), 66061552(10/24/2026), 66074999(10/4/2026), 66075318(11/19/2026), 66104892(10/21/2026), 66104893(10/22/2026), 66104894(10/23/2026), 66104895(11/13/2026), 66108277(11/15/2026), 66118638(11/22/2026), 66120310(10/29/2026), 66120312(10/30/2026), 66120313(10/31/2026), 66127027(11/15/2026), 66127028(11/20/2026), 66132570(11/21/2026), 66132571(11/25/2026), 66132572(11/27/2026), 66140447(11/2/2026), 66140448(11/5/2026), 66140449(11/6/2026), 66140450(11/7/2026), 66142269(11/28/2026), 66142274(11/29/2026), 66151008(12/20/2026), 66160820(11/30/2026), 66160821(12/3/2026), 66160822(12/4/2026), 66160823(12/5/2026), 66174935(12/6/2026), 66186389(12/9/2026), 66186390(12/10/2026), 66186391(12/11/2026), 66186393(12/19/2026), 66214346(12/12/2026), 66214347(12/17/2026), 66214348(12/13/2026), 66214349(12/16/2026), 66225263(1/24/2027), 66230833(1/27/2027), 66230834(1/28/2027), 66231174(1/29/2027), 66236300(2/3/2027), 66243301(1/30/2027), 66243302(2/1/2027), 66254697(2/4/2027), 66254698(2/10/2027), 66273573(2/11/2027), 66273574(2/12/2027), 66283862(2/8/2027), 66296222(3/5/2027), 66315689(3/6/2027), 66351811(3/8/2027), 66351812(3/11/2027), 66351813(3/12/2027), 66378395(3/13/2027), 66378396(3/18/2027), 66384489(3/18/2027), 66414674(3/22/2027), 66438179(4/3/2027), 66438197(4/12/2027), 66438198(5/24/2027), 66438199(5/27/2027), 66438200(4/10/2027), 66439368(3/26/2027), 66439369(3/31/2027), 66439370(4/2/2027), 66439371(4/7/2027), 66439372(4/9/2027), 66488597(5/28/2027), 66521743(4/16/2027), 66529338(4/15/2027), 66529339(4/21/2027), 66529340(4/22/2027), 66529341(4/23/2027), 66529345(5/23/2027), 66544240(4/24/2027), 66594945(5/14/2027), 66597237(4/29/2027), 66597238(4/30/2027), 66597239(5/10/2027), 66601166(5/2/2027), 66601167(5/8/2027), 66601168(5/12/2027), 66601169(5/13/2027), 66601170(5/14/2027), 66601171(5/29/2027), 66642726(5/9/2027), 66692566(6/6/2027), 66704724(6/4/2027), 66710839(6/2/2027), 66710840(6/3/2027), 66739812(6/13/2027), 66739813(6/18/2027), 66739814(6/17/2027), 66739910(6/24/2027), 66739911(7/17/2027), 66739912(7/9/2027), 66739913(6/16/2027), 66739916(6/23/2027), 66740114(7/17/2027), 66758828(7/10/2027), 66767282(6/28/2027), 66769651(7/18/2027), 66782067(7/21/2027), 66826029(7/23/2027), 66826030(7/24/2027), 66832079(7/25/2027), 66844048(7/31/2027), 66873884(8/2/2027), 66873885(8/5/2027), 66873886(8/18/2027), 66895223(8/20/2027), 66938771(8/22/2027), 66938772(8/26/2027), 66938773(8/27/2027), 66964710(9/1/2027), 66964711(9/4/2027), 66982688(9/26/2027), 67025469(10/20/2027), 67047800(10/17/2027), 67047801(10/21/2027), 67068446(10/28/2027), 67092101(10/28/2027), 67098252(10/30/2027), 67098253(11/3/2027), 67199591(11/12/2027), 67199595(11/13/2027), 67199596(11/11/2027), 67199617(11/21/2027), 67199618(11/22/2027), 67217934(1/7/2028), 67217935(12/4/2027), 67266297(1/12/2028), 67275624(12/20/2027), 67275626(12/3/2027), 67322713(1/13/2028), 67322714(1/16/2028), 67357488(1/29/2028), 67395549(2/5/2028), 67395555(1/28/2028), 66739917(6/12/2027); 131F7/00690103000405/ 65902900(8/1/2026), 65902901(8/3/2026), 65910728(8/2/2026), 65910729(7/29/2026), 65910730(7/27/2026), 65910731(7/25/2026), 65910732(7/26/2026), 65910735(7/30/2026), 65910736(8/24/2026), 65910737(7/31/2026), 65916927(8/3/2026), 65916928(8/6/2026), 65916929(8/7/2026), 65916930(8/8/2026), 65916931(8/9/2026), 65916932(8/22/2026), 65916933(8/23/2026), 65944791(8/20/2026), 65944792(8/21/2026), 65955857(9/9/2026), 65955858(9/17/2026), 65955859(9/26/2026), 65955860(9/27/2026), 65973739(9/5/2026), 65973740(9/6/2026), 65973741(9/7/2026), 65973742(9/10/2026), 65988571(9/28/2026), 65997478(9/16/2026), 65997479(9/17/2026), 65997481(9/19/2026), 65997482(9/20/2026), 66010504(9/10/2026), 66010505(9/11/2026), 66010506(9/12/2026) ,66010507(9/13/2026) ,66010508(9/14/2026) ,66023074(9/30/2026) ,66033088(10/5/2026) ,66048930(10/9/2026), 66057629(10/6/2026), 66057630(10/8/2026), 66057944(10/15/2026), 66057945(10/17/2026), 66061552(10/24/2026), 66074999(10/4/2026), 66075318(11/19/2026), 66104892(10/21/2026), 66104893(10/22/2026), 66104894(10/23/… (truncated, 14046 characters total — see the official FDA record for the full value)
Recalling firm:
Becton, Dickinson and Company
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 8, 2026

SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS. Model Numbers: SDA-SYS-3000-2D-HTC, SDA-SYS-3000-3D, SDM-SYS-6000-2D, SDM-SYS-6000-3D, SDM-00001-2D, SDM-00001-3D, SDM-00001-M2D, SDM-00001-M3D, SDM-05000-2A2, SDM-05000-2A3, SDM-05000-2AC, SDM-05000-2D2, SDM-05000-2D3, SDM-05000-2DC, SDM-05000-3D2, SDM-05000-3D3, SDM-05000-3DC, SDM-SYS-9000-2D, SDM-SYS-9000-3D.

Complaints have been received of systems developing loose, missing, or broken internal bolts over time.

ALL 50 STATES
▸Full report

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

Recall #:
98566
Lot/product code:
"Model No.; UDI": [SDA-SYS-3000-2D-HTC;15420045510616], [SDA-SYS-3000-3D;15420045517783], [SDM-SYS-6000-2D;15420045510753], [SDM-SYS-6000-3D;15420045510760], [SDM-00001-2D;15420045510623], [SDM-00001-3D;15420045510630], [SDM-00001-M2D;15420045510647], [SDM-00001-M3D;15420045510654], [SDM-05000-2A2;15420045510661], [SDM-05000-2A3;15420045510678], [SDM-05000-2AC;15420045510685], [SDM-05000-2D2;15420045510692], [SDM-05000-2D3;15420045510708], [SDM-05000-2DC;15420045510715], [SDM-05000-3D2;15420045510722], [SDM-05000-3D3;15420045510739], [SDM-05000-3DC;15420045510746], [SDM-SYS-9000-2D;15420045510777], [SDM-SYS-9000-3D;15420045510784]; All Serial No.
Recalling firm:
Hologic, Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 8, 2026

Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P

Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.

ALL 50 STATES
▸Full report

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

Recall #:
98603
Lot/product code:
Model-UDI-DI(Expiration): SGPT755P/00690103219388/65869018(6/24/2026), 66010501(9/23/2026), 67122784(10/28/2027); SGPT54/00690103219289/65956343(8/19/2026); SGPT64P/00690103219371
Recalling firm:
Becton, Dickinson and Company
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 7, 2026

BD GasPak EZ Campy Pouch System. Catalog Number: 260685. for microbiologic use

BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce carbon dioxide levels below specification.

ALL 50 STATES
▸Full report

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

Recall #:
98657
Lot/product code:
Catalog Number: 260685; UDI-DI: 30382902606858; Lot Number: 5329863.
Recalling firm:
Becton Dickinson & Co.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled April 7, 2026

Alendronate Sodium Oral Solution, 70 mg/75 mL, 75 mL, Rx only, 4 x 75 mL Single Dose Bottles, Distr. by: Hikma Pharmaceuticals USA Inc., Berkeley Heights, NJ 07922, NDC 0054-0282-59.

This recall is being conducted due to not meeting quality requirements assay results in a limited number of bottles that were stored on side.

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-0526-2026
Lot/product code:
Lot # AC2040A, Exp Date: 04/2026
Recalling firm:
Hikma Pharmaceuticals USA INC
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled April 7, 2026

Lidocaine Wound Gel (Benzalkonium Chloride, 0.13% and Lidocaine Hydrochloride, 2%), NET WT 0.5 OZ (14 g), Distributed by: CVS PHarmacy, INc., One CVS Drive, Woonsocket, RI 02895. NDC 59898-950

Failed PH Specifications

ALL 50 STATES
▸Full report

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:
D-0509-2026
Lot/product code:
Lots: A5014, A5018, A5019
Recalling firm:
Water-Jel Technologies, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodAllergenMilkUndeclaredRecalled April 7, 2026

Bulk Horchata Powder 3951 (100547) 1/25 HORCHATA UPC: 042743-19015-0 Item: 100547

Not listed on the label milk.

AKALARAZCACOFLIAIDILINKSLAMIMNMOMTNENMNVOHOKORTNTXUTVAWAWI
▸Full report

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

Recall #:
H-0672-2026
Lot/product code:
Lot, Expiration: HR02224, 01/23/26; HR06124, 03/05/26; HR16524, 06/14/26; HR23624, 08/27/26; HR34124, 12/11/26; HR07125, 03/13/27; HR09025, 04/03/27; HR23425, 08/27/27; HR34425, 12/15/27; HR01926, 01/28/28.
Recalling firm:
Marquez Brothers International, Inc.
View official FDA record (opens in a new tab)