Official U.S. recalls · explained plainly

Know if it’s recalled — and exactly what to do.

We pull official government recall records and translate each one into plain language: what happened, how serious it is, and the steps to take. No legalese.

Search by meaning, not just keywords — describe the product or the hazard and we’ll find matching recalls even when the official notice uses different words. Brand names and model numbers work too.

Latest recalls

76,825 found

⛔ Stop using nowConsumer product
Haier America Recalls 42-inch LED-TVs Due to Risk of Injury
Haier recalls 42-inch LED TVs with model LE42B1380 due to TV stand neck support breaking, which can cause tipping and injury. Consumers must stop using and return the TV to get a free replacement stand neck.
HaierOct 2, 2012
⛔ Stop using nowConsumer product
Fitness Anywhere Recalls Early Model Suspension Trainer Devices Due to Fall Hazard
Fitness Anywhere recalls early Professional (P1) and Tactical (T1) Suspension Trainer devices (2006-2007) due to strap buckle failure risking falls. Affected units have yellow/khaki anchor straps with specific markings.
Fitness AnywhereOct 2, 2012
ℹ️ UnratedDrug
ITW Dymon recalls Lemon Hand Sanitizing Wipes [n-alkyl dimethyl benzyl ammonium chloride (0.1%) and n-alkyl dimethyl ethyl benzyl
ITW DymonSep 28, 2012
ℹ️ UnratedDrug
Fresenius Kabi USA, LLC recalls ONDANSETRON INJECTION, USP, 4 mg/ 2 mL (2 mg/mL), For IM or IV Use, Single Dose 2 mL Vials, Rx only. APP
Fresenius Kabi USA, LLCSep 27, 2012
ℹ️ UnratedDrug
Dr. Reddy's Laboratories, Inc. recalls Dr. Reddy's Quetiapine Fumarate Tablets, 25mg, Rx Only, 500 tablets. Mfd By: Dr. Reddy's Laboratories Limited,

Know if it’s recalled — and exactly what to do.

Latest recalls

Haier America Recalls 42-inch LED-TVs Due to Risk of Injury

Fitness Anywhere Recalls Early Model Suspension Trainer Devices Due to Fall Hazard

ITW Dymon recalls Lemon Hand Sanitizing Wipes [n-alkyl dimethyl benzyl ammonium chloride (0.1%) and n-alkyl dimethyl ethyl benzyl

Fresenius Kabi USA, LLC recalls ONDANSETRON INJECTION, USP, 4 mg/ 2 mL (2 mg/mL), For IM or IV Use, Single Dose 2 mL Vials, Rx only. APP

Dr. Reddy's Laboratories, Inc. recalls Dr. Reddy's Quetiapine Fumarate Tablets, 25mg, Rx Only, 500 tablets. Mfd By: Dr. Reddy's Laboratories Limited,

Genentech, Inc. recalls CellCept (mycophenolate mofetil) capsules, 250 mg, packaged in a) 12 x 120-count bottles per carton, NDC 0004-0259-05;

Fresenius Kabi USA, LLC recalls MIDAZOLAM HYDROCHLORIDE INJECTION, 5 mg/1 mL, C-IV, For IM or IV Use, 2 mL Vials, Rx only. APP Pharmaceuticals, LLC.

Fresenius Kabi USA, LLC recalls CYANOCOBALAMIN INJECTION, USP, 1000 mcg/mL, For IM or IV Use, Multiple Dose 2 mL Vials, Rx only. APP Pharmaceuticals,

Cyclone Swing Seats Recalled by ADS Due to Fall Hazard

Captain Cutlass Pirate Toy Guns Recalled by Dillon Importing Due to Violation of Lead Paint Standard

Cabot Recalls Wood Cleaner and Wood Brightener With Spray Pump Due To Irritation and Burn Hazard

Atomic Aquatics Recalls Cobalt Dive Computer Due to Impact and Drowning Hazard

New England Compounding Center recalls Hyaluronidase 150 u/ml PF, 1 mL, 5 mL, and 10 mL vials, manufactured by New England Compounding Center, Framingham, MA

New England Compounding Center recalls Dexamethasone Sodium Phosphate 4 mg/mL vials PF, 6 mg/mL PF vials, and 8 mg/mL PF vials, manufactured by New England

New England Compounding Center recalls Methylprednisolone Acetate 80 mg/mL Injection, Preserved, supplied in 5 mL and 10 mL vials, manufactured by New England

New England Compounding Center recalls Lidocaine/Dextrose 5%/7.5% PF, manufactured by New England Compounding Center, Framingham, MA

New England Compounding Center recalls Clonidine 100 mcg/mL PF, 1mL and 2 mL vials, manufactured by New England Compounding Center, Framingham, MA

New England Compounding Center recalls Methylprednisolone Acetate (PF) 80 mg/ml Injection, supplied in 1 mL, 2 mL and 5 mL vials, manufactured by New England

New England Compounding Center recalls Bupivacaine 0.25% PF, Bupivacaine 0.5% PF, and Bupivacaine 0.75% PF, manufactured by New England Compounding Center,

New England Compounding Center recalls Betamethasone Sodium Phosphate 6 mg/mL P Injection, Betamethasone Sodium Phosphate 6 mg/mL PF Injection, Betamethasone

New England Compounding Center recalls Betamethasone Repository 6 mg/mL PF Injection and Betamethasone Repository 6 mg/mL P Injection, manufactured by New

New England Compounding Center recalls Lidocaine 1% PF, 2% PF, and 4% PF, in 1 mL, 2 mL, 5 mL, and 10 mL vials, manufactured by New England Compounding

New England Compounding Center recalls Triamcinolone 10 mg/mL P, 40mg/mL P, 40mg/mL PF and 80 mg/mL PF in 1 mL, 2 mL, 5 mL, and 10 mL vials, manufactured by

New England Compounding Center recalls Saline 10% and 3%, in 5 mL and 10 mL vials, manufactured by New England Compounding Center, Framingham, MA

New England Compounding Center recalls Omnipaque 240mg/mL PF, 300mg/mL PF, in 3 mL, 5 mL, and 10 mL, vials, manufactured by New England Compounding Center,

New England Compounding Center recalls Isovue 200 mg/mL PF and 300 mg/mL PF, Vials, manufactured by New England Compounding Center, Framingham, MA

New England Compounding Center recalls Methylprednisolone Acetate 40 mg/mL Injection, Preserved, supplied in 5 mL and 10 mL vials, manufactured by New England

New England Compounding Center recalls Glycerin 100% PF, 1mL, 2 mL, and 5 mL vials, manufactured by New England Compounding Center, Framingham, MA

New England Compounding Center recalls Methylprednisolone Acetate (PF) 40 mg/ml Injection, supplied in 1 mL, 2 mL and 5 mL vials, manufactured by New England

Big Lots Recalls Garden Swings Due to Fall Hazard