State

Maine product recalls

73,584 recalls have nationwide distribution and so reach Maine. 3,922 additional recalls listed Maine specifically in their distribution scope.

What the numbers show

Total: 3,922
Critical: 478
Severe: 964
Most recent: 2026-09-23

Of the 3,922 recalls naming Maine we have scored against our rubric, 478 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 964 (25%) are Severe.

Which agencies issued them

These figures cover only the 3,922 recalls whose distribution notice names Maine specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

776–800 of 77506

HighFDA (Devices)·Z-3058-2026·2026-09-09
Medline Pre-Op Kits Recalled for Potential Sterility Breach
Medline is recalling 13,032 pre-operative kits nationwide due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Product
Medline Convenience Kits: 1) PRE-OP KIT, Catalog Number: DYKS1043F; 2) PRE OP KIT, Catalog Number: DYKS1128C; 3) PRE OP KIT, Catalog Number: DYKS1216I; 4) PRE OP KIT, Catalog Number: DYKS1325A; 5) CATARACT PREOP KIT, Catalog Number: DYKS1583; 6) GENERAL PREOP KIT…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3071-2026·2026-09-09
Medline IV Start Kits Recalled Due to Potential Seal Defects
Medline is recalling IV start kits containing BD ChloraPrep applicators with potentially open or incomplete seals, which may lead to infection.
Product
Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators IV START KIT LAB DRAW-SH CDS860014Q IV START KIT DYKM1000B IV START KIT LAB DRAW-SH CDS860014P ULTRASOUND GUIDED PIV START KI DYNDV2684
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3076-2026·2026-09-09
Medline Convenience Kits Recalled for Potential Applicator Seal Defects
Medline is recalling specific lots of Convenience Kits containing BD ChloraPrep Clear applicators due to potential packaging seal defects that could lead to infection.
Product
Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators LABOR CDS CDS981762B VAG DELIVERY ADMISSION BAG DYKA1054F
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3049-2026·2026-09-09
Medline Convenience Kits Recalled for Potential Sterility Breach
Medline is recalling 4,636 convenience kits nationwide due to packaging wrinkles that may compromise sterility, posing a risk of microbial contamination.
Product
Medline Convenience Kits: 1) CDS840396X, Catalog Number: CDS840396X; 2) CDS840396Y, Catalog Number: CDS840396Y; 3) CDS983348AA, Catalog Number: CDS983348AA; 4) CDS983348AB, Catalog Number: CDS983348AB; 5) CDS983672O, Catalog Number: CDS983672O; 6) CDS983672P, Catalog…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0823-2026·2026-09-09
Allies Group Recalls Subpotent SPF 50 Sunscreen Gel Nationwide
Allies Group Inc. is recalling 29,014 tubes of THE ONE SPF 50 Invisible Sunscreen Gel because testing showed the product may not provide the labeled SPF 50 protection.
Product
THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 50ML - 1.7 fl. oz Tube, Made in U.S.A, Distributed by Allies Group Pte Ltd, Singapore 068914. UPC 8 885014 073224
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0824-2026·2026-09-09
Allies Group Recalls Subpotent SPF 50 Sunscreen Gel Sachets
Allies Group Inc. is recalling 27,492 sachets of THE ONE SPF 50 Invisible Sunscreen Gel because firm testing indicated the product may not reliably provide the stated SPF 50 protection.
Product
THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 3ml - 0.1 fl. oz, Sachet: Single use only, Made in the U.S.A, Distributed by Allies Group Pte Ltd, Singapore 068914.UPC 8 885014 073293
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3092-2026·2026-09-09
Fresenius NaturaLyte Liquid Acid Concentrate Recalled for Discoloration
Fresenius Medical Care is recalling NaturaLyte Liquid Acid Concentrate for Bicarbonate Hemodialysis due to reports of blue-green discoloration in the product.
Product
NaturaLyte, Liquid Acid Concentrate for Bicarbonate Hemodialysis: Product Numbers: 08-1251-1, 08-2251-0, 08-2301-3, 08-3251-9, 08-3301-2, 13-2201-5, 13-2251-0, 13-3251-9; Liquid Acid Concentrate for Bicarbonate Hemodialysis
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3103-2026·2026-09-09
Cardinal Health Recalls Urinary Catheter Trays with Potentially Contaminated Wipes
Cardinal Health is recalling 175 units of Presource Packs containing CliniClean Pericare Wipes due to potential lubricant contamination that may cause localized skin effects.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) PBCGLVBLI, Catalog Number: KIT, BLO LAVH ; 2) PB15HYFCY, Catalog Number: KIT, UMMC AB HYST II 170032 ; 3) SMA4FTLSCA, Catalog Number: TLH PACK
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3095-2026·2026-09-09
Cardinal Health Recalls Presource Packs with Potentially Contaminated Wipes
Cardinal Health 200, LLC is recalling 846 Presource Packs containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant, posing a risk of localized skin irritation.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, GYN ROBOTIC GSAM , Catalog Number: PBCCGRSGD; 2) KIT, GYN ROBOT ACCESSORY , Catalog Number: PB35GYBJC; 3) KIT, PRIMARY RESECTION , Catalog Number: PGVMOTBB19…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0816-2026·2026-09-09
Baxter Recalls Clindamycin Phosphate Injection Due to CGMP Deviations
Baxter Healthcare is voluntarily recalling Clindamycin Phosphate Injection due to Current Good Manufacturing Practice (CGMP) deviations. The affected product was distributed in the US, Puerto Rico, and Chile.
Product
CLINDAMYCIN PHOSPHATE — CLINDAMYCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3105-2026·2026-09-09
Cardinal Health Recalls Urinary Catheter Trays with Contaminated Wipes
Cardinal Health is recalling 44 units of urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, CHONY ORTHO MAJOR SPINE , Catalog Number: POV2SCCPP; 2) KIT,ORTHOPLASTIC MICROVASCULAR, Catalog Number: PWVMFFABLI
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0822-2026·2026-09-09
Bionpharma Recalls Doxylamine Succinate Tablets Due to Foreign Material Presence
Bionpharma Inc. is recalling Doxylamine Succinate and Pyridoxine HCl tablets because foreign tablets or capsules were found in the product.
Product
DOXYLAMINE SUCCINATE AND PYRIDOXINE HYDROCHLORIDE — DOXYLAMINE SUCCINATE AND PYRIDOXINE HYDROCHLORIDE (DOXYLAMINE SUCCINATE AND PYRIDOXINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3104-2026·2026-09-09
Cardinal Health Recalls Surgical Kits with Potentially Contaminated Wipes
Cardinal Health is recalling 645 surgical kits containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, ASLMC CRANIOTOMY , Catalog Number: PNCGCNAUM; 2) KIT, ORP MAJOR SPINE , Catalog Number: PNHDFSVCI; 3) KIT,ORP NEURO TRAUMA , Catalog Number: PNHDOTVCQ…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3100-2026·2026-09-09
Cardinal Health Recalls Urinary Catheter Trays with Potentially Contaminated Wipes
Cardinal Health is recalling 61 units of urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, ENT HARVEST , Catalog Number: PEVMETBJX; 2) KIT, ENT HARVEST , Catalog Number: PEVMETB37
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3096-2026·2026-09-09
Cardinal Health Recalls Urinary Catheter Trays with Contaminated Wipes
Cardinal Health is recalling 19 units of urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, LUNG TX CIRCULATOR , Catalog Number: OVC3507231
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3093-2026·2026-09-09
Fresenius Citrasate Liquid Acid Concentrate Recalled for Discoloration
Fresenius Medical Care is recalling Citrasate Liquid Acid Concentrate for Bicarbonate Hemodialysis due to complaints of blue-green discoloration.
Product
Citrasate, Liquid Acid Concentrate for Bicarbonate Hemodialysis: Product Numbers: 08-2251-CA, 08-3251-CA, 13-2251-CA; Liquid Acid Concentrate for Bicarbonate Hemodialysis
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3097-2026·2026-09-09
Cardinal Health Recalls Urinary Catheter Trays with Contaminated Wipes
Cardinal Health is recalling 115 units of urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT,ROBOTICS DH , Catalog Number: PGOCRDNHD; 2) KIT, EAS ROBOTIC , Catalog Number: PG36RPEAB; 3) KIT, VIDEO THORACOSCOPY CMC , Catalog Number: PVCGVTACF
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3098-2026·2026-09-09
Cardinal Health Recalls Urinary Catheter Trays with Potentially Contaminated Wipes
Cardinal Health is recalling 2,448 urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant, posing a risk of localized skin irritation.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, GVI OPEN HEART A B , Catalog Number: PCVNCG540; 2) KIT, GVI OPEN HEART A B , Catalog Number: PCVNCG542; 3) KIT, GVI OPEN HEART A B , Catalog Number: PCVNCG55I…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0825-2026·2026-09-09
Allies Group Recalls Subpotent Sunscreen Gel Due to Inadequate SPF Protection
Allies Group Inc. is recalling specific lots of THE ONE SPF 50 Invisible Sunscreen Gel because testing showed the product may not provide the labeled SPF 50 protection.
Product
THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 20ml - 0.7 fl. oz. Tube, Made in the U.S.A, Distributed by Allies Group Pte Ltd, Singapore 068914. UPC 8 885014 074733
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0826-2026·2026-09-09
Allies Group Recalls Subpotent SPF 50 Sunscreen Gel
Allies Group Inc. is recalling 2,149 tubes of SPF 50 sunscreen gel because testing showed it may not provide the labeled sun protection.
Product
THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 90ml - 3 fl. oz. Tube, Made in the U.S.A, Distributed by Allies Group Pte Ltd, Singapore 068914. UPC 8 885014 075853
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3047-2026·2026-09-09
Diagnostica Stago Recalls STA Staclot Protein S Reagent Due to QC Drift
Diagnostica Stago is recalling 5,220 units of STA Staclot Protein S reagent because quality control values drifted within the stated stability period.
Product
STA Staclot Protein S, Model/Catalog Number: 00746-Reagent Lot number 273074; qualitative and quantitative factor deficiency test
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3102-2026·2026-09-09
Cardinal Health Recalls Urinary Catheter Trays with Contaminated Wipes
Cardinal Health is recalling specific urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, ROBOTIC HYST , Catalog Number: PB41RHRM3; 2) KIT, ROBOTIC HYST , Catalog Number: PB41RHRM4; 3) KIT, C SECTION , Catalog Number: PLVMCS22G…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3099-2026·2026-09-09
Cardinal Health Recalls Urinary Catheter Trays with Contaminated Wipes
Cardinal Health is recalling 60 units of urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT,MAXILLOFACIAL PRESBYTERIAN, Catalog Number: PWV2MF01D
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0812-2026·2026-09-09
Baxter Recalls Pantoprazole Sodium Infusion Bags Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Pantoprazole Sodium infusion bags due to Current Good Manufacturing Practice (CGMP) deviations.
Product
PANTOPRAZOLE SODIUM — PANTOPRAZOLE SODIUM (PANTOPRAZOLE SODIUM IN 0.9% SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0830-2026·2026-09-09
Mylan Recalls Mycophenolate Mofetil Injection Due to Dissolution Failures
Mylan Pharmaceuticals is recalling Mycophenolate Mofetil for injection because it failed to meet dissolution specifications.
Product
MYCOPHENOLATE MOFETIL — MYCOPHENOLATE MOFETIL (MYCOPHENOLATE MOFETIL)
Category
Drug
Distribution
Distributed nationwide