Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

1126–1150 of 114834

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 (Drugs)·D-0828-2026·2026-09-09
Lexia LLC Recalls Broadway Joe's Pain Cream Due to CGMP Deviations
Lexia LLC is recalling Broadway Joe's Pain Cream in Colorado due to CGMP deviations and potential raw material contamination.
Product
Broadway Joe's Pain Cream, (Histamine Dihydrochloride 0.025%), 1500mg CBD Isolate, 1000mg Hempseed oil, 2 oz-jar, Produced for Broadway Joe's, Franklin, TN, 37067, NDC 83088-8120-5, UPC 8 50041 64003 7
Category
Drug
Distribution
1 state
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 (Food)·H-1324-2026·2026-09-09
Wonton Specialist Dumpling Skin Recalled for Undeclared Red Dye
Wonton Specialist Inc. is recalling 16 oz bags of Dumpling Skin due to undeclared FD&C Red No. 40. The product was distributed in New York, New Jersey, and Pennsylvania.
Product
Wonton Specialist Inc. Dumpling Skin, 16 oz - packaged in foam tray overwrapped with clear plastic
Category
Food
Distribution
3 states
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 (Food)·H-1325-2026·2026-09-09
Wonton Specialist Cooked Noodle Recalled for Undeclared Red Dye
Wonton Specialist is recalling 700 bags of cooked noodles in New York, New Jersey, and Pennsylvania due to undeclared FD&C Red No. 40.
Product
Wonton Specialist Inc. Cooked Noodle, 16 oz and 5 lb - packaged in clear plastic bags
Category
Food
Distribution
3 states
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
ModerateFDA (Food)·H-1321-2026·2026-09-09
Wonton Noodle Recalled for Undeclared FD&C Red No. 40
Wonton Specialists is recalling 550 bags of Wonton Noodle in New York, New Jersey, and Pennsylvania due to undeclared FD&C Red No. 40.
Product
Wonton Specialist Inc. Wonton Noodle, 12 oz - packaged in foam tray overwrapped with clear plastic and 5lb - packaged in clear plastic bags
Category
Food
Distribution
3 states
ModerateFDA (Drugs)·D-0839-2026·2026-09-09
Mylan Recalls Prasugrel Tablets for Failed Dissolution and Stability Testing
Mylan Pharmaceuticals is recalling 47,662 bottles of Prasugrel 10mg tablets because they failed dissolution specifications and 18-month stability testing.
Product
PRASUGREL — PRASUGREL (PRASUGREL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3094-2026·2026-09-09
Cardinal Health Recalls Presource Packs with Potential Lubricant Contamination
Cardinal Health is recalling 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) KIT,GYN LAPAROSCOPY DH , Catalog Number: PBOCGLN17
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3101-2026·2026-09-09
Cardinal Health Recalls Presource Packs with Potentially Contaminated Wipes
Cardinal Health 200, LLC is recalling 1,398 Presource Packs 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, BLO ROBOTIC GYN , Catalog Number: PBCGRGB28; 2) KIT , GYN MAJOR BARNES JEWIS, Catalog Number: PBVMLP22G; 3) KIT, GYN OPERATIVE LAPAROSCOPY, Catalog Number: PBVM0722D…
Category
Medical Device
Distribution
Distributed nationwide

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1126–1150 of 114834