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Recalls affecting Arizona

Data last updated: September 8, 2026 at 1:13 PM UTC

16,936 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/virusAnnounced 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/virusAnnounced 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)
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)
UnclassifiedAllergenUndeclaredAnnounced 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)
UnclassifiedBacteria/virusAnnounced 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/virusAnnounced 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 April 27, 2026

Medline convenience kits: BASIC DYNJ905869G BASIC PACK DYNJ68484B BIB GENERAL LAPAROSCOPY PA DYNJ58305 CHRISTUS CH PEDIATRIC BASIC DYNJ61167G CVC INSERTION BUNDLE CVI3940A DAVINCI PACK SURGICOUNT DYNJ45544F EPCH BASIC PACK DYNJ83094C GENERAL PACK DYNJ39682B DYNJ84882 GENERAL RFD DYNJ906336F GENERAL SURGERY PACK DYNJT6003 GV MACD PACK DYNJ46952M IMPLANT PACK - BBI AR DYNJ63508A KIT THORACOSCOPY DYNJ908872F LVAD TRAY DM1120A MAJOR UROLOGY PACK-LF DYNJ0368525M MICRODISECT DECOMPRESS-LF DYNJ911467 MINOR PACK DYNJ86972 MULTI PURPOSE PACK DYNJ58406B OPEN HEART DYNJ903245C P&K PACK DYNJT5838 PACK,PEDIATRIC MAJOR DYNJ906888F PCNL DYNJ904468C PEDIATRIC MINOR RFD DYNJ906296I PEDIATRIC PACK DYNJ54239K PEDIATRIC SURGERY DYNJ81474B PERLMUTTER PACK DYNJT7387 RFT ISC NOBLES MINOR PACK DYNJ43954B ROBOTICS FMOL LADY OF THE LAKE DYNJ89584 ROBOTICS PACK DYNJ83622B SCOLI PACK NTX DYNJ68415C SMALL ABDOMINAL PACK-LF PHS41749G STIM IMPLANT TRIALS DYNJ87790A SUPPLEMENTAL PACK DYNJ65244 TENEX PACK DYNDH2190 THORACIC PACK DYNJ56616G THORACIC PACK SHD DYNJ68416C THORACOSCOPY DYNJ9425843R THORACOTOMY PM DYNJ906815A THORACOTOMY THORACOSCOPY DYNJ902882D TRAY,NEONATAL PICC DRSG CHANGE DYNDC1533B UNIVERSAL-ASC DYNJ900071C

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

ALL 50 STATES
Full report

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

Recall #:
98951
Lot/product code:
DYNJ905869G UDI-DI 10198459394577 Lot 25JBX559 DYNJ68484B UDI-DI 10198459368967 Lot 25LME889 DYNJ58305 UDI-DI 10889942843763 Lot 25KBA708 DYNJ61167G UDI-DI 10198459386671 Lots 25KBN904 25LBQ928 CVI3940A UDI-DI 10653160998976 Lot 26AME675 DYNJ45544F UDI-DI 10193489876130 Lot 25KBJ042 DYNJ83094C UDI-DI 10198459562051 Lot 25JMD330 DYNJ39682B UDI-DI 10193489769241 Lots 25KBI410 25LBI978 26BBC735 DYNJ84882 UDI-DI 10195327432324 Lot 26CBQ487 DYNJ906336F UDI-DI 10198459419959 Lots 25KBR497 26CBO946 DYNJT6003 UDI-DI 10198459531255 Lots 25JBV850 26CBC211 DYNJ46952M UDI-DI 10198459090134 Lots 25KBH401 25LBO238 DYNJ63508A UDI-DI 10193489363845 Lot 26BBC181 DYNJ908872F UDI-DI 10198459660306 Lot 26BBR620 DM1120A UDI-DI 10653160998891 Lots 25KBA425 25LBJ075 DYNJ0368525M UDI-DI 10193489820249 Lots 25KBG895 25KBG896 DYNJ911467 UDI-DI 10198459358562 Lot 25LBA393 DYNJ86972 UDI-DI 10195327694296 Lot 26CBD230 DYNJ58406B UDI-DI 10193489957228 Lot 25JBT217 DYNJ903245C UDI-DI 10889942890170 Lot 26ABG614 DYNJT5838 UDI-DI 10198459513329 Lot 25JBT808 DYNJ906888F UDI-DI 10198459194764 Lot 26AMC879 DYNJ904468C UDI-DI 10195327631413 Lot 25KBL838 DYNJ906296I UDI-DI 10198459419829 Lot 25KBN303 DYNJ54239K UDI-DI 10198459443206 Lot 25LMG373 DYNJ81474B UDI-DI 10198459100260 Lot 25JBY253 DYNJT7387 UDI-DI 10198459615924 Lot 26CBQ932 DYNJ43954B UDI-DI 10193489509168 Lot 25LMI928 DYNJ89584 UDI-DI 10198459278723 Lots 25JBS433 25LBO815 25LBP820 DYNJ83622B UDI-DI 10198459402739 Lots 25JBA251 25JBX613 DYNJ68415C UDI-DI 10195327341749 Lots 25KBM185 26BBD267 PHS41749G UDI-DI 10198459438844 Lot 25LMG971 DYNJ87790A UDI-DI 10198459358968 Lots 25KBC718 25KBC975 DYNJ65244 UDI-DI 10193489257434 Lots 25KBC479 26CBC173 DYNDH2190 UDI-DI 10198459467967 Lots 25KBE086 25KBM732 DYNJ56616G UDI-DI 10198459533167 Lots 25LBD705 26CBC585 DYNJ68416C UDI-DI 10195327341688 Lot 25KBH744 DYNJ9425843R UDI-DI 10198459085499 Lot 25KMC242 DYNJ906815A UDI-DI 10195327027018 Lot 26BBO802 DYNJ902882D UDI-DI 10198459496790 Lot 25LBR117 DYNDC1533B UDI-DI 10889942813926 Lot 25JBU460 DYNJ900071C UDI-DI 10198459121722 Lots 26AMH365 26AMH758
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

BDSpinal Tray with BDWhitacre Needle 25 G x 3.5 in., BDQuincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405741.

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.

ALL 50 STATES
Full report

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

Recall #:
98842
Lot/product code:
Catalog Number: 405741. UDI Number: (01)00382904057411(17)261001(10)B02V204D. Lot Number (Expiration Date): B02V204D (2026-10-01).
Recalling firm:
Becton Dickinson & Company
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

BDSpinal Tray with BDWhitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405645.

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.

ALL 50 STATES
Full report

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

Recall #:
98842
Lot/product code:
Catalog Number: 405645. UDI Numbers: (01)00382904056452(17)261001(10)B01V223D. Lot Number (Expiration Date): B01V223D (2026-10-01).
Recalling firm:
Becton Dickinson & Company
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

Medline convenience kits: ACL PACK DYNJ64161C ARTHROSCOPY PACK DYNJ47103D DYNJ67197G DYNJ85197A DYNJT4007 BASIC ACCESS PACK-LF DYNJ36698B BASIC BACK TRAY DYNJ89037 BASIC PEDI PACK-LF DYNJ0171446I DYNJ0171446J BASIC SPINE DYNJ910915A BREAST PACK DYNJ87587A BREAST PLASTIC PACK DYNJ84482C C SECTION DYNJ49172I CAROTID ENDARTERECTOMY PACK DYNJ48013L CENTRAL LINE PACK-LF DYNJ0220136S CERVICAL FUSION DYNJ908135B CERVICAL SPINE PACK DYNJ53044G C-SECTION DYNJ909099F DAVINCI PROSTATE PACK DYNJ61711C DEPAUL FOOT & ANKLE-LF DYNJ20010L DIEP PACK DYNJ64964J DYNJ43210K DYNJ61787F DYNJ87065 EAR CUSTOM PACK DYNJ82564A ENT FREE FLAP PACK SAFETY DYNJ54720D EP PACEMAKER SAFETY #1 DYNJ54722F EPCH EXTREMITY PACK DYNJ83095B EXTREMITY PACK DYNJ32934F EXTREMITY PACK-LF DYNJ68935B FISTULA PACK DYNJ66502B GENDER AFFIRMING SURGERY DYNJ66252F GYN LAPAROSCOPY PACK AHSC DYNJT8381 HAND PACK WATCHMAKER-LF DYNJ34580D HEAD & NECK PACK-LF DYNJ0282388T DYNJ88308 HIP SCOPE DYNJ907120D KNEE ARTHRO PACK DYNJ58404F KNEE ARTHROSCOPY PACK DYNJ84740A LAMI OVERHEAD PACK DYNJ46531Q LAMINECTOMY NEURO MPH DYNJT5271 LAMINECTOMY PACK DYNJ68785D LAP APPY PACK DYNJT6005 LAP CHOLE PACK DYNJ82087A LEVY PACK DYNJ83939C MAJOR LAP VCH DYNJ39217P MAJOR NEURO PACK-LF DYNJ0578916AA MAJOR PACK DYNJ58528J MINOR GEN PACK DYNJ61661B MINOR LAPAROTOMY PACK-LF DYNJ0753436P MINOR PACK DYNJ54968B NEURO PACK DYNJ67628D NEURO SHUNT PACK-LF DYNJ0578815W OMFS PACK DYNJ54400C OPEN HEART PACK DYNJT5008 OPEN HEART-LF DYNJ48260F OPEN LAPAROTOMY PACK DYNJ39247I DYNJ39247J PACEMAKER PACK DYNJ31461I DYNJ61411C PACK,ORTHO FLIP DYNJ65471B PED OPEN HEART PACK DYNJ45373G PLASTIC PACK DYNJ82495D PLASTICS PK - NO SYR DYNJ62433F PODIATRY PACK OP7809M PPE BUNDLE KIT DT13351A PROSTATE ROBOTIC PACK DYNJ84120C RADIAL ART LINE INSERTION ARTNC234 ROBOTIC GENERAL WHH DYNJT5376 ROBOTIC PACK DYNJ47978G RR-SPINE PACK DYNJ62643B SHOULDER ARTH PACK DYNJ58410D SHOULDER ARTHROSCOPY PACK DYNJ54477C DYNJT8391 SHOULDER PACK DYNJ61052B DYNJT3266 SHOULDER PACK-LF DYNJ0122428K PHS656414I SPINE PACK DYNJ64949C DYNJ83649B SPINE SHOULDER PACK DYNJ47104D STERILE ACCESS KIT DYNDA2664 TOTAL KNEE PACK DYNJ84741B TUBAL PACK DYNJ68253F UNIVERSAL PACK DYNJ83246B VA TAMPA GENERAL ROBOTIC PACK DYNJT6993 W.C. MINOR LAPAROTOMY PK-LF DYNJ0509186J ZALE OTOLOGY CDS CDS983181G

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

ALL 50 STATES
Full report

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

Recall #:
98951
Lot/product code:
DYNJ64161C UDI-DI 10198459146961 Lot 25KBH332 DYNJ47103D UDI-DI 10198459625008 Lot 25LMF684 DYNJ67197G UDI-DI 10198459481994 Lot 25JBA258 DYNJ85197A UDI-DI 10198459217395 Lot 25LMF727 DYNJT4007 UDI-DI 10198459381867 Lot 26BBC180 DYNJ36698B UDI-DI 10198459081811 Lots 25KBM204 26CBD413 DYNJ89037 UDI-DI 10198459229855 Lots 25KBI083 25KBM202 DYNJ0171446I UDI-DI 10195327589516 Lot 25JBT239 DYNJ0171446J UDI-DI 10198459591754 Lot 26CBB295 DYNJ910915A UDI-DI 10198459424960 Lot 25LBD596 DYNJ87587A UDI-DI 10198459114199 Lot 25JBR735 DYNJ84482C UDI-DI 10198459362491 Lot 26BBU043 DYNJ49172I UDI-DI 10198459042003 Lot 26AMA388 DYNJ48013L UDI-DI 10198459560941 Lot 25LBP624 DYNJ0220136S UDI-DI 10198459566073 Lot 25LMF648 DYNJ908135B UDI-DI 10198459586552 Lots 25LBC200 25LBR878 DYNJ53044G UDI-DI 10198459448768 Lot 25LMG369 DYNJ909099F UDI-DI 10198459375996 Lot 25JMF136 DYNJ61711C UDI-DI 10198459096754 Lot 25JBT124 DYNJ20010L UDI-DI 10198459229053 Lot 25JMD853 DYNJ64964J UDI-DI 10198459254109 Lot 25LMI867 DYNJ43210K UDI-DI 10198459546792 Lot 25LMI070 DYNJ61787F UDI-DI 10198459169694 Lot 25JBU635 DYNJ87065 UDI-DI 10198459007439 Lots 25KBD819 25LBP631 DYNJ82564A UDI-DI 10198459497551 Lot 25LBD560 DYNJ54720D UDI-DI 10195327549510 Lot 26CBC228 DYNJ54722F UDI-DI 10195327549633 Lots 25KBB967 25LBQ696 26CBE680 DYNJ83095B UDI-DI 10198459562068 Lot 25JMD325 DYNJ32934F UDI-DI 10195327697181 Lot 26CBC762 DYNJ68935B UDI-DI 10198459440373 Lot 25LBN254 DYNJ66502B UDI-DI 10198459395321 Lot 25KBC481 DYNJ66252F UDI-DI 10198459185397 Lot 25LBP873 DYNJT8381 UDI-DI 10198459702358 Lot 26CBD354 DYNJ34580D UDI-DI 10195327579661 Lot 25LMF989 DYNJ0282388T UDI-DI 10198459591990 Lot 25LBP896 DYNJ88308 UDI-DI 10198459143328 Lot 25KBJ822 DYNJ907120D UDI-DI 10198459427985 Lots 25KBK051 25KBT376 26DBF975 DYNJ58404F UDI-DI 10198459366413 Lots 25KBI176 26CBE677 DYNJ84740A UDI-DI 10198459421556 Lot 25KBB657 DYNJ46531Q UDI-DI 10198459526107 Lot 25LMJ845 DYNJT5271 UDI-DI 10198459471452 Lot 25LBC165 DYNJ68785D UDI-DI 10198459546952 Lot 25JBU924 DYNJT6005 UDI-DI 10198459531187 Lot 25JBU086 DYNJ82087A UDI-DI 10198459078019 Lot 25LMH034 DYNJ83939C UDI-DI 10198459342523 Lot 25JBY263 DYNJ39217P UDI-DI 10198459102356 Lot 25JME213 DYNJ0578916AA UDI-DI 10198459117565 Lot 25JME873 DYNJ58528J UDI-DI 10198459322815 Lot 26CBE343 DYNJ61661B UDI-DI 10198459096785 Lot 25KBA722 DYNJ0753436P UDI-DI 10198459466854 Lot 25LMJ282 DYNJ54968B UDI-DI 10198459428753 Lot 25KBD827 DYNJ67628D UDI-DI 10198459383373 Lot 25LMG428 DYNJ0578815W UDI-DI 10198459466892 Lot 25LMI628 DYNJ54400C UDI-DI 10195327646905 Lot 25KBI070 DYNJT5008 UDI-DI 10198459463525 Lot 26BBC492 DYNJ48260F UDI-DI 10198459220241 Lot 25KBL822 DYNJ39247I UDI-DI 10195327633509 Lot 25JBR808 DYNJ39247J UDI-DI 10198459640698 Lot 26BBD397 DYNJ31461I UDI-DI 10198459519734 Lot 25JBV372 DYNJ61411C UDI-DI 10198459493591 Lot 25KBA043 DYNJ65471B UDI-DI 10198459168574 Lot 25JMF211 DYNJ45373G UDI-DI 10198459254635 Lot 25LMI203 DYNJ82495D UDI-DI 10198459439834 Lots 25KBI927 25LBR381 DYNJ62433F UDI-DI 10198459627514 Lot 25LBO801 OP7809M UDI-DI 10198459368493 Lot 26CBB615 DT13351A UDI-DI 10653160325581 Lots 25JBA293 25KBB632 DYNJ84120C UDI-DI 10198459574177 Lot 26AMA032 ARTNC234 UDI-DI 10198459566974 Lot 25KBJ985 DYNJT5376 UDI-DI 10198459470783 Lot 25LBP929 DYNJ47978G UDI-DI 10198459416606 Lot 26AMA586 DYNJ62643B UDI-DI 10198459164446 Lot 25LMG407 DYNJ58410D UDI-DI 10198459366468 Lot 25LBI975 DYNJ54477C UDI-DI 10198459004155 Lot 25LMI210 DYNJT8391 UDI-DI 10198459703140 Lot 26CBJ555 DYNJ61052B UDI-DI 10198459421587 Lot 26BBC156 DYNJT3266 UDI-DI 10198459320965 Lot 25LMH283 DYNJ0122428K UDI-DI 10198459533297 Lot 25EBP843A PHS656414I UDI-DI 10198459006258 Lot 25LMG515 DYNJ64949C UDI-DI 10198459190216 Lot 25LMH829 DYNJ83649B UDI-DI 10198459110177 Lot 25KBC046 DYNJ47104D UDI-DI 10198459624964 Lot 25LMJ846 DYNDA2664 UDI-DI 10193489342635 Lots 25JBT011 26CBD503 DYNJ84741B UDI-DI 10198459421563 Lot 25KBC487 DYNJ68253F UDI-DI 10198459185366 Lot 25KBA720 DYNJ83246B UDI-DI 10195327665463 Lots 25KBN031 25LBQ952 DYNJT6993 UDI-DI 10198459588211 Lot 25KBI629 DYNJ0509186J UDI-DI 10198459117626 Lot 25LMI076 CDS983181G UDI-DI 10198459038174 Lot 25LBA047
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

BDSpinal Tray with BDWhitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405671.

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.

ALL 50 STATES
Full report

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

Recall #:
98842
Lot/product code:
Catalog Number: 405671. UDI Number: (01)00382904056711(17)270101(10)B01V275D. Lot Number (Expiration Date): B01V275D (2027-01-01). ***Expansion 07/08/2026 UDI Number: (01)00382904056711(17)270101(10)B01V294D; Lot Number (Expiration Date): B01V294D (2027-01-01).
Recalling firm:
Becton Dickinson & Company
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled April 27, 2026

Primidone Tablets, USP, 250 mg, 100-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-638-01

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

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-0535-2026
Lot/product code:
Lot #: GS067909, Exp 4/30/2028; GS068646, Exp 8/31/2026
Recalling firm:
Golden State Medical Supply Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled April 27, 2026

Ascend Laboratories, LLC, Metoprolol Succinate Extended-Release Tablets, USP, 25 mg* Rx Only, Manufactured by: Alkem Laboratories Ltd., India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-590-01.

Failed Dissolution Specifications

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-0547-2026
Lot/product code:
Lot # 25140859; Exp. Date: Jan 2027
Recalling firm:
Ascend Laboratories, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

Medline convenience kits: ADD-A-CATH ARTERIAL INSERTION ARTNC185 PED SCHOOL AGE PICC DRSG TRAY DYNDC3291

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

ALL 50 STATES
Full report

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

Recall #:
98951
Lot/product code:
ARTNC185 UDI-DI 10195327640729 Lot 25JBU463 DYNDC3291 UDI-DI 10195327334741 Lot 25KBH082
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

BDSpinal Tray with BDWhitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400868, 405652.

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.

ALL 50 STATES
Full report

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

Recall #:
98842
Lot/product code:
1. Catalog Numbers: 400868. UDI Numbers: (01)10885403469510(17)261001(10)B01V206D, (01)10885403469510(17)261001(10)B01V220D, (01)10885403469510(17)270101(10)B02V266D. Lot Number (Expiration Date): B01V206D (2026-10-01), B01V220D (2026-10-01), B02V266D (2027-01-01). 2. Catalog Number: 405652. UDI Numbers: (01)00382904056520(17)270130(10)B01V353D, (01)00382904056520(17)270101(10)B02V267D. Lot Numbers (Expiration Date): B01V353D (2027-01-30), B02V267D (2027-01-01).
Recalling firm:
Becton Dickinson & Company
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

Brand Name: Silent Nite Product Name: Silent Nite Sleep Appliance Model/Catalog Number: SILNT Product Description: Silent Nite Sleep Appliance is a mandibular advancement device (MAD) intended to treat snoring and mild to moderate obstructive sleep apnea (OSA).

Due to device not having FDA Clearance

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Full report

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

Recall #:
98834
Lot/product code:
Item Number: NITESL UDI-DI code: D745SILNT0 Lot/Serial Numbers: 1020214577 1020784354 1030007997 1030439672 1030523763 1030722759 1106770735 1107310424 1107642834 1108530251 1110784932 1117400787 1118814629 1121913952 1122251905 1122958036 1124408531 1125495087 1127571733 1131149684
Recalling firm:
Prismatik Dentalcraft, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

BDSpinal Tray with BDQuincke Needle 26 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405632.

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.

ALL 50 STATES
Full report

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

Recall #:
98842
Lot/product code:
Catalog Number: 405632. UDI Number: (01)00382904056322(17)270101(10)B01V231D; Lot Number (Expiration Date): B01V231D (2027-01-01). ***Expansion 07/08/2026 UDI Number: (01)00382904056322(17)270101(10)B02V248D; Lot Number (Expiration Date): B02V248D (2027-01-01).
Recalling firm:
Becton Dickinson & Company
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

Medline convenience kit: BHS NEURO DYNJ904900N MEDTRX NEURO PACK DYNJ67267B MRI DBS PACK DYNJ9814630O NEURO CDS-LF CDS983383L NEURO PACK DYNJ59397Q DYNJT7315 NEURO PACK-LF DYNJ25097I NEURO VP SHUNT/VAGAL NERVE-RF DYNJ21925S PK NEURO SHUNT BUMC DYNJT6428 RR-NEURO DBS HEAD PACK-LF DYNJ0785736M VP SHUNT SYNJ10307B

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

ALL 50 STATES
Full report

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

Recall #:
98951
Lot/product code:
DYNJ904900N UDI-DI 10198459504273 Lot 25LBB457 DYNJ67267B UDI-DI 10198459084331 Lot 25LBQ732 DYNJ9814630O UDI-DI 10195327587291 Lot 25LBD665 CDS983383L UDI-DI 10198459224577 Lot 25LBC092 DYNJ59397Q UDI-DI 10198459495427 Lot 25LMG049 DYNJT7315 UDI-DI 10198459620225 Lot 25LBO095 DYNJ25097I UDI-DI 10198459449550 Lot 25KBC747 DYNJ21925S UDI-DI 10195327105020 Lots 25KBD835 25LBR371 DYNJT6428 UDI-DI 10198459553660 Lot 26AMA602 DYNJ0785736M UDI-DI 10198459487149 Lot 25LMI831 SYNJ10307B UDI-DI 10195327007249 Lot 25LBE309
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

Medline EBSI Kit EBSI1534

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

ALL 50 STATES
Full report

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

Recall #:
98951
Lot/product code:
UDI-DI 10653160350507 Lot 2025110490
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

Medline convenience kit: SMSC-PELVISCOPY PACK-LF DYNJ0161619M

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

ALL 50 STATES
Full report

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

Recall #:
98951
Lot/product code:
UDI-DI 10198459028274 Lot 25LMI820
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

BDSpinal Tray with BDQuincke Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405621, 405735.

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.

ALL 50 STATES
Full report

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

Recall #:
98842
Lot/product code:
1. Catalog Number: 405621. UDI Numbers: (01)00382904056216(17)260601(10)B01V142D, (01)00382904056216(17)260628(10)B01V176D. Lot Numbers (Expiration Date): B01V142D (2026-06-01), B01V176D (2026-06-28). 2. Catalog Number: 405735. UDI Numbers: (01)00382904057350(17)260601(10)B01V149D, (01)00382904057350(17)261001(10)B01V190D. Lot Numbers (Expiration Date): B01V149D (2026-06-01), B01V190D (2026-10-01).
Recalling firm:
Becton Dickinson & Company
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

Medline convenience kits: DAVINCI DYNJ905836D DAVINCI-LF DYNJ905293I GENERAL ROBOTICS PACK DYNJT8308 GYN LAP CDS860087Q GYN LAPAROSCOPY DYNJ910084C GYN LAPAROSCOPY CDS CDS982371I GYN LAPAROSCOPY CDS #34-RF CDS920099S GYN LAPAROSCOPY PACK DYNJT3887 DYNJT6876 GYN ROBOTIC CDS CDS984228K GYN ROBOTICS DYNJ911843 KIT LABOR DELIVERY TUBAL LIGAT DYKMBNDL165C ROBOTIC LAP CHOLE CDS CDS985442J ROBOTIC PACK DYNJ84725B DYNJ910594B ROBOTIC SURGERY PACK DYNJ53711B ROBOTICS PACK DYNJ83622C UOFL GYN LAPAROSCOPY DYNJ909322B WMC ROBOTIC PACK - LF DYNJ902583O

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

ALL 50 STATES
Full report

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

Recall #:
98951
Lot/product code:
DYNJ905836D UDI-DI 10195327517977 Lot 25LBB534 DYNJ905293I UDI-DI 10198459247972 Lot 25KBM585 DYNJT8308 UDI-DI 10198459697135 Lot 26CBD040 CDS860087Q UDI-DI 10198459543005 Lots 25JBV094 25LBP061 DYNJ910084C UDI-DI 10198459597466 Lot 25LBE810 CDS982371I UDI-DI 10198459044106 Lots 25KBH343 26CBN241 CDS920099S UDI-DI 10195327140656 Lot 25KBO172 DYNJT3887 UDI-DI 10198459366871 Lot 25JBX564 DYNJT6876 UDI-DI 10198459583148 Lot 25KBM646 CDS984228K UDI-DI 10198459044113 Lot 26ABF608 DYNJ911843 UDI-DI 10198459555206 Lot 25LBC203 DYKMBNDL165C UDI-DI 10198459634284 Lot 25LBR024 CDS985442J UDI-DI 10198459476686 Lot 25JBT926 DYNJ84725B UDI-DI 10198459366949 Lot 25JBA329 DYNJ910594B UDI-DI 10198459563768 Lot 25KBJ104 DYNJ53711B UDI-DI 10198459023538 Lots 25KBF929 25LBB875 DYNJ83622C UDI-DI 10198459607172 Lots 25LBR740 26CBJ460 DYNJ909322B UDI-DI 10198459443848 Lot 25LBD961 DYNJ902583O UDI-DI 10198459441806 Lot 25LBC041
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

Aligned Medical AMS16835 Fluids Kit RX

Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits.

ALL 50 STATES
Full report

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

Recall #:
98957
Lot/product code:
UDI-DI: B098AMS168350; Lot Numbers: 233828, 236048, 236359, 236662, 238580, 239934, 239935
Recalling firm:
Windstone Medical Packaging, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

Medline convenience kits: C-SECTION KIT DYNJ904305J C-SECTION PACK DYNJ69533C

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

ALL 50 STATES
Full report

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

Recall #:
98951
Lot/product code:
DYNJ904305J UDI-DI 10198459268151 lot 25KBT972 DYNJ69533C UDI-DI 10198459524097 lot 26BBC483
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

BDSpinal Tray with BDWhitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405637, 405707.

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.

ALL 50 STATES
Full report

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

Recall #:
98842
Lot/product code:
1. Catalog Number: 405637. UDI Numbers: (01)00382904056377(17)260628(10)B01V160D, (01)00382904056377(17)270101(10)B01V241D, (01)00382904056377(17)270101(10)B01V265D, (01)00382904056377(17)261001(10)B02V183D. Lot Numbers (Expiration Date): B01V160D (2026-06-28), B01V241D (2027-01-01), B01V265D (2027-01-01), B02V183D (2026-10-01). 2. Catalog Number: 405707. UDI Number: (01)00382904057077(17)270101(10)B02V230D. Lot Number (Expiration Date): B02V230D (2027-01-01).
Recalling firm:
Becton Dickinson & Company
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

Medline convenience kit: (82)LABOR & DELIVERY C-SECTION DYNJ907895F

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

ALL 50 STATES
Full report

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

Recall #:
98951
Lot/product code:
UDI-DI 10198459366390 Lot 25KBL873
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

BDSpinal Tray with BDWhitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405658.

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.

ALL 50 STATES
Full report

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

Recall #:
98842
Lot/product code:
Catalog Number: 405658. UDI Number: (01)00382904056582(17)261001(10)B01V217D. Lot Number (Expiration Date): B01V217D (2026-10-01).
Recalling firm:
Becton Dickinson & Company
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH DYNJ63276G

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

ALL 50 STATES
Full report

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

Recall #:
98951
Lot/product code:
DYNJ84775A UDI-DI 10195327606527 lot 25LMH070 DYNJ47269D UDI-DI 10195327674786 lot 25LMJ234 DYNJ63276G UDI-DI 10198459458835 lot 26BBC598
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled April 27, 2026

Primidone Tablets, USP, 50 mg, 50-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-637-05

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

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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-0534-2026
Lot/product code:
Lot#: GS066750, GS067084, GS067710, GS067873, Exp 3/31/2028; GS068339, GS068897, Exp 8/31/2028
Recalling firm:
Golden State Medical Supply Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

Medline convenience kits: ACD DYNJ904999J ACDF DYNJ907336B DYNJ910821A ACDF PACK DYNJ81098C ACL DYNJ911996 ACL ACCESSORY PACK DYNJ86584B ACL- LF DYNJ905281B ACL PACK DYNJ67271A ALIF DYNJ904848L ANTERIOR CERVICAL DYNJ901355J ARTHROSCOPY DYNJ908193B ARTHROSCOPY PACK-LF DYNJ42963M DYNJ52268B ARTHROSCOPY SHOULDER DYNJ908684A BACK CDS-LF CDS983364G BACK PACK DYNJT4339 CDH SPINE PACK DYNJ908828D CERVICAL CDS DYNJ903477J CMC ORTHO BACK TRAY SYNJ10272B CRANIOTOMY DYNJ911853 CRANIOTOMY ROOSEVELT PACK DYNJ58358F CUSTOM HAND PACK-LF DYNJ0537135V CUSTOM SPINAL PACK DYNJT7544 DISCECTOMY PACK DYNJ86770 DJ ORTHO SPINE DYNJ48980M EXTREMITY PACK-LF DYNJT4161 FOOT PACK DYNJ53179D GENERAL ORTHO-ACNW DYNJ84891 GILMORE SHOULDER SCOPE PACK DYNJ58002 GV LUMBAR LAMINECTOMY PK DYNJ46938L HAND PACK DYNJ63113B DYNJ69662A DYNJT5855 HAND-LF DYNJ903263B KIT LAMINECTOMY DYNJ908806C KNEE ARTHROSCOPY DYNJ902056C DYNJ904846I KNEE ARTHROSCOPY-LF DYNJ905871F KNEE SCOPE DYNJ906986G LAMINECTOMY DYNJ904847K DYNJ909505D LAMINECTOMY CDS CDS983115K LAMINECTOMY CERVICAL DISC-LF DYNJ905286G LAMINECTOMY NEURO PACK DYNJ58356F LAMINECTOMY SPINE DYNJ904139L LOWER EXTREMITY PACK DYNJ63114C LUMBAR CERVICAL PACK-LF DYNJ0101088G LUMBAR LAMI DYNJ905020J LUMBAR LAMINECTOMY DYNJ53707 LUMBAR LAMINECTOMY PACK DYNJT4386 MAIN/LAMINECTOMY PACK-LF DYNJ0565499AN NJ SPINE SPECIALIST PACK DYNJ58706F OHOW SPINE-BACK PACK DYNJ910097A ORTHO NECK CDS-LF CDS983134C ORTHO PACK-LF DYNJ37202G ORTHO SPINE DYNJ40221G OSC BEACH CHAIR SHOULDER-LF DYNJ905282C PACC PETRIE ACL ADD ON PACK-LF DYNJ58290D PACK,ARTHROSCOPY ASC DYNJ65484A PACK,POSTERIOR SPINAL FUSION DYNJ906892B PAD LATERAL SPINE DYNJ902158L DYNJ902158M PAD POSTERIOR SPINE DYNJ902142L PK-SPINE DYNJ58259A PODIATRY PACK DYNJ62288D POST SPINE PACK DYNJ20509R POSTERIOR SPINAL FUSION DYNJ903250B RFT ARTHROSCOPY PACK DYNJ43956C RFT SHOULDER PACK-NOBLE DYNJ36331D SA SHOULDER #2 BORDEN DYNJ56501A SHOULDER DYNJ900893M DYNJ904184I SHOULDER ARTHROSCOPY DYNJ904842G SHOULDER PACK DYNJ83483 SHOULDER PACK-LF DYNJ42973N SHOULDER SCOPE PACK NTX DYNJ68399C SPINAL PACK DYNJ49692G SPINE DYNJ910451A SPINE PACK DYNJ20147O DYNJ84971 DYNJ86044A DYNJ86308C DYNJ88917 DYNJS3069 DYNJT4163 DYNJT8396 ST CHARLES TOTAL HIP DYNJ909593C TOTAL HIP DYNJ910906D TOTAL HIP PACK DYNJ64156B TOTAL JOINT DYNJ904186G TOTAL KNEE PACK DYNJ60967 DYNJ61409A WMC ORTHO SPINE WMC-LF DYNJ902528M XLIF DYNJ910795B

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

ALL 50 STATES
Full report

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

Recall #:
98951
Lot/product code:
DYNJ904999J UDI-DI 10195327305024 lot 26DBJ301 DYNJ907336B UDI-DI 10198459084300 lot 26DBF966 DYNJ910821A UDI-DI 10198459453359 lots 25KBH623 26BBL877 26BBM089 DYNJ81098C UDI-DI 10198459357107 lots 25JBR783 25KBD860 DYNJ911996 UDI-DI 10198459596230 lots 25LBI311 25LBV123 26ABN955 DYNJ86584B UDI-DI 10198459410604 lot 25LMH561 DYNJ905281B UDI-DI 10195327063191 lot 25KBD109 DYNJ67271A UDI-DI 10195327626822 lot 25JBV609 DYNJ904848L UDI-DI 10198459217500 lot 26DBK390 DYNJ901355J UDI-DI 10198459224775 lot 25LBK865 DYNJ908193B UDI-DI 10198459521720 lot 25LBD958 DYNJ42963M UDI-DI 10198459611834 lot 26AMB027 DYNJ52268B UDI-DI 10195327432423 lots 25LBC027 26CBA143 DYNJ908684A UDI-DI 10198459500510 lot 26AMH337 CDS983364G UDI-DI 10195327432508 lot 26BBR233 DYNJT4339 UDI-DI 10198459448720 lot 26CBC179 DYNJ908828D UDI-DI 10198459512919 lots 25KMC466 26AMG065 DYNJ903477J UDI-DI 10195327565206 lots 26AMG182 26AMG272 SYNJ10272B UDI-DI 10195327006532 lot 25LBO306 DYNJ911853 UDI-DI 10198459559372 lot 25KBI658 DYNJ58358F UDI-DI 10198459105029 lots 25JBX146 25LBP519 DYNJ0537135V UDI-DI 10195327556389 lots 25KBG081 25LBP178 26BBC915 DYNJT7544 UDI-DI 10198459631399 lots 25LBN779 DYNJ86770 UDI-DI 10195327674229 lot 25KBJ623 DYNJ48980M UDI-DI 10195327533694 lot 25LMK166 DYNJT4161 UDI-DI 10198459410741 lot 25JBA211 DYNJ53179D UDI-DI 10198459574658 lot 25LMH296 DYNJ84891 UDI-DI 10195327434151 lot 25JBT703 DYNJ58002 UDI-DI 10889942807383 lot 25LBO695 DYNJ46938L UDI-DI 10198459090103 lot 25JBS479 DYNJ63113B UDI-DI 10195327131449 lot 25KBJ559 DYNJ69662A UDI-DI 10198459132360 lot 25JBX052 DYNJT5855 UDI-DI 10198459515057 lots 25JBV938 25LBO691 DYNJ903263B UDI-DI 10889942754014 lot 26CBQ083 DYNJ908806C UDI-DI 10198459285868 lot 25LMJ639 DYNJ902056C UDI-DI 10195327422103 lots 25JBU940 25LBR965 DYNJ904846I UDI-DI 10198459217579 lot 26CBS964 DYNJ905871F UDI-DI 10198459206252 lot 25LBA302 DYNJ906986G UDI-DI 10198459610226 lot 26AMJ169 DYNJ904847K UDI-DI 10198459217586 lot 25KBR022 DYNJ909505D UDI-DI 10198459594229 lot 25LMJ127 CDS983115K UDI-DI 10198459579608 lot 25LBE987 DYNJ905286G UDI-DI 10198459248184 lots 26AMA067 26AMH307 DYNJ58356F UDI-DI 10198459104923 lot 25LBR764 DYNJ904139L UDI-DI 10198459528583 lot 25JBT916 DYNJ63114C UDI-DI 10193489870206 lot 25JBX122 DYNJ0101088G UDI-DI 10198459619960 lot 25LBQ608 DYNJ905020J UDI-DI 10198459548314 lot 25KBJ908 DYNJ53707 UDI-DI 10889942441082 lots 25LBP985 26CBR371 DYNJT4386 UDI-DI 10198459457609 lot 25KBK189 DYNJ0565499AN UDI-DI 10195327318352 lot 25JMF339 DYNJ58706F UDI-DI 10198459124877 lot 26CBC852 DYNJ910097A UDI-DI 10198459504785 lot 26AMD592 CDS983134C UDI-DI 10195327147655 lot 25KBT474 DYNJ37202G UDI-DI 10195327685393 lots 25JBS464 25LBR525 DYNJ40221G UDI-DI 10198459448515 lot 25LMJ294 DYNJ905282C UDI-DI 10195327393069 lot 25KBM844 DYNJ58290D UDI-DI 10195327513467 lot 25LBQ039 DYNJ65484A UDI-DI 10195327303501 lot 25LMB980 DYNJ906892B UDI-DI 10198459168611 lots 25KBG661 26BBC906 DYNJ902158L UDI-DI 10198459453021 lot 25LBD928 DYNJ902158M UDI-DI 10198459681721 lot 26DBK385 DYNJ902142L UDI-DI 10198459452970 lot 25LBA949 DYNJ58259A UDI-DI 10193489734034 lots 25JBY406 25LBM865 DYNJ62288D UDI-DI 10195327605827 lots 25JBA294 25KBB258 DYNJ20509R UDI-DI 10198459277849 lots 25LMH654 26AMB105 DYNJ903250B UDI-DI 10889942755288 lot 25KBM855 DYNJ43956C UDI-DI 10193489970708 lot 25KBL821 DYNJ36331D UDI-DI 10198459416446 lot 25LMH136 DYNJ56501A UDI-DI 10195327310752 lot 25LMI162 DYNJ900893M UDI-DI 10198459408632 lots 25KMB298 26AMB284 DYNJ904184I UDI-DI 10198459640704 lot 26CBO500 DYNJ904842G UDI-DI 10198459217753 lot 25LBC835 DYNJ83483 UDI-DI 10195327268916 lot 25KBH325 DYNJ42973N UDI-DI 10198459621178 lot 26AMA642 DYNJ68399C UDI-DI 10195327341763 lot 26BBD183 DYNJ49692G UDI-DI 10195327347352 lot 26AMA587 DYNJ910451A UDI-DI 10198459365560 lot 25KBG700 26ABF330 DYNJ20147O UDI-DI 10198459377617 lot 25JBA158 DYNJ84971 UDI-DI 10195327442620 lot 26BBC185 DYNJ86044A UDI-DI 10198459404351 lot 25LBQ169 DYNJ86308C UDI-DI 10198459425233 lot 25LBQ110 DYNJ88917 UDI-DI 10198459215926 lot 25LMF333 DYNJS3069 UDI-DI 10888277058286 lot 25LBC215 DYNJT4163 UDI-DI 10198459410758 lot 26BBC139 DYNJT8396 UDI-DI 10198459704871 lot 26CBE087 DYNJ909593C UDI-DI 10198459523816 lot 25LBB787 DYNJ910906D UDI-DI 10198459472626 lot 25KBJ090 DYNJ64156B UDI-DI 10195327678746 lots 25KBC275 25LBC916 26CBC871 DYNJ904186G UDI-DI 10198459002922 lots 25KBG639 25LBB568 DYNJ60967 UDI-DI 10193489537918 lot 25LMJ893 DYNJ61409A UDI-DI 10193489778595 lots 25LMH863 26AMC051 DYNJ902528M UDI-DI 10198459445873 lot 25KBU092 DYNJ910795B UDI-DI 10198459594205 lot 25LMH707
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 27, 2026

Medline convenience kits: DRIVELINE MANAGEMENT KIT EBSI1688 PORT DRESSING CHANGE KIT EBSI1328A

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

ALL 50 STATES
Full report

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

Recall #:
98951
Lot/product code:
EBSI1688 UDI-DI 10653160370130 Lot 2025102890 EBSI1328A UDI-DI 10653160382980 Lot 2025103090
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)