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Recall archive

94,421 stored notices, from Jun 20, 2012 to Sep 26, 2026.

31,892 recalls · page 185 of 1329

Drugs

Reported Jan 24, 2025

Provepharm Inc. recalls Provepharm Inc. Phenylephrine hydrochloride Injection, USP, 10 mg/ mL due to Device & Drug Safety – Potential Foreign Material

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Provepharm Inc.

FDA (recalls & safety alerts)

Food

Reported Jan 24, 2025

TS FOOD PACKAGING recalls Wabash Valley Farms, Rural King Bacon flavor popcorn seasoning due to Potential or Undeclared Allergen – soy

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Ts Food Packaging

FDA (recalls & safety alerts)

Consumer products

Reported Jan 23, 2025

NQDTPBOR Helmets Recalled Due to Risk of Head Injury; Violation of Federal Regulations for Bicycle Helmets; Sold…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

CLSYS International Inc.

CPSC

Consumer products

Reported Jan 23, 2025

Duluth Trading Company Recalls Children's Holiday Pajama Sets Due to Burn Hazard; Violation of Federal Flammability…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Duluth Holdings Inc., dba Duluth Trading Company

CPSC

Consumer products

Reported Jan 23, 2025

GiantMouse Recalls GM12 and GMP12 Folding Knives Due to Laceration Hazard

High riskUsing this product could cause serious injury, illness or death — stop using it now.

GiantMouse LLC

CPSC

Consumer products

Reported Jan 23, 2025

ChrisDowa Roller Window Shades Recalled Due to Strangulation and Entanglement Hazards; Violation of Federal Regulations…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Shaoxingkeqiao Nenghaozhenfang Co. Ltd.

CPSC

Consumer products

Reported Jan 23, 2025

SHEIN Distribution Corporation Recalls Teckwe Hair Dryer Brushes Due to Electrocution or Shock Hazard

High riskUsing this product could cause serious injury, illness or death — stop using it now.

SHEIN Distribution Corporation

CPSC

Medical devices

Reported Jan 22, 2025

McKesson Cardiology Hemo software

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

A L I Technologies Ltd.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 22, 2025

Wicklow Gold Cheddar Nettle & Chive Cheese, 5.2 oz., plastic cryo-vac , 8 packages per case

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Abbey Specialty Foods

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 22, 2025

Impella RP with SmartAssist; Product Number: 0046-0035;

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Abiomed, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

VerifyNow P2Y12 Platelet Reactivity Test, REF: 85064

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Accriva Diagnostics, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jan 22, 2025

Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117,…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Akron Pharma, Inc.

6 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 22, 2025

Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Model/Catalog Number: 8065977763 Product Description:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alcon Research LLC

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Jan 22, 2025

Clobazam Tablets, 10 mg, packaged in 30 tablets per carton (3x10 blister cards each), Rx Only, Amneal Pharmaceuticals…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Amerisource Health Services LLC

1 more product in this recall

FDA (openFDA drug enforcement)

Food

Reported Jan 22, 2025

Apna Wholesale Inc recalls Paras Premium Golden Raisins due to Undeclared Sulfites

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Apna Wholesale Inc.

FDA (recalls & safety alerts)

Medical devices

Reported Jan 22, 2025

Augustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Single Port, Models: 1) Model #…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Augustine Temperature Management, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Welch Allyn, Inc., Life 2000 Ventilation System, REF BT-20-0002

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Baxter Healthcare Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Idylla INSTRUMENT, IVD, REF P0010. Intended for the detection of nucleic acid targets in various types of human…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biocartis Nv

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

ACCOLADE DR Pacemaker, SL (Model Number L301), SL MRI (Model Number L311), EL (Model Number L321), and EL MRI (Model…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Boston Scientific Corporation

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Cardinal Health Presource Kits: 1) KIT,PLASTIC FLAP,Catalog Number PGHDOT951; 2) KIT,ORP PLASTIC FLAP,Catalog Number…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cardinal Health 200, LLC

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

BD Pyxis MedStation ES (Med ES Main), REF: 323; and BD Pyxis MedStation ES (Med ES Main Tower), REF: 352

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Folysil Silicone Foley Catheters, Device Reference Numbers AA6106, AA6108, AA6110, AA6112, AA6114, AA6116, AA6118,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Coloplast Manufacturing US, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Esteem Synergy Stomahesive Skin Barrier, part of Esteem synergy, which is a two-piece ostomy system consisting of an…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ConvaTec, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Cook Medical Biodesign Otologic Butterfly Graft, REF ENT-OTO-BFLY-0.4-0.6, REF G60285, Sterile.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cook Biotech, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

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