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

ℹ️ UnratedDrug
Performance Plus Marketing, Inc. recalls BLUE Diamond PLATINUM Capsules, 1000 mg, supplied in 1, 5 and 10 count blister packs, Distributed By: DH Distribution
Performance Plus Marketing, Inc.Dec 17, 2012
ℹ️ UnratedDrug
Performance Plus Marketing, Inc. recalls BLUE Diamond Pill, supplied in 1, 5 and 10 count blister packs, Male Sexual Enhancement, Distributed By: DH
Performance Plus Marketing, Inc.Dec 17, 2012
⛔ Stop using nowConsumer product
Dunecraft Recalls Water Balz, Skulls, Orbs and Flower Toys Due to Serious Ingestion Hazard
Dunecraft recalls marble-sized toys that expand in the body after ingestion, causing intestinal blockages. These Water Balz, Growing Skulls, H2O Orbs and Fabulous Flowers toys require immediate removal from children and replacement.
DunecraftDec 17, 2012
ℹ️ UnratedDrug
Mylan Institutional, Inc. (d.b.a. UDL Laboratories) recalls Hydrocodone Bitartrate and Acetaminophen Tablets, USP, 10 mg/500 mg; 100 Tablets (5 x 20), 5 cards each containing 20
Mylan Institutional, Inc. (d.b.a. UDL Laboratories)Dec 14, 2012
ℹ️ UnratedDrug
Watson Laboratories Inc recalls Caziant (desogestrel and ethinyl estradiol) Tablets, USP, (Triphasic Regimen), 0.1 mg/0.025 mg, 0.125 mg/0.025 mg, 0.15
Watson Laboratories IncDec 13, 2012

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

Latest recalls

Performance Plus Marketing, Inc. recalls BLUE Diamond PLATINUM Capsules, 1000 mg, supplied in 1, 5 and 10 count blister packs, Distributed By: DH Distribution

Performance Plus Marketing, Inc. recalls BLUE Diamond Pill, supplied in 1, 5 and 10 count blister packs, Male Sexual Enhancement, Distributed By: DH

Dunecraft Recalls Water Balz, Skulls, Orbs and Flower Toys Due to Serious Ingestion Hazard

Mylan Institutional, Inc. (d.b.a. UDL Laboratories) recalls Hydrocodone Bitartrate and Acetaminophen Tablets, USP, 10 mg/500 mg; 100 Tablets (5 x 20), 5 cards each containing 20

Watson Laboratories Inc recalls Caziant (desogestrel and ethinyl estradiol) Tablets, USP, (Triphasic Regimen), 0.1 mg/0.025 mg, 0.125 mg/0.025 mg, 0.15

Mattresses Recalled by Easy-Rest Due to Violation of Federal Mattress Flammability Standard

Enesco Recalls Shelly's Diner Collectible Due to Fire Hazard

American Mattress Manufacturing Recalls Renovated Mattresses Due to Violation of Federal Flammability Standard

Boehringer Ingelheim Roxane Inc recalls Perindopril Erbumine Tablets, 8mg, 100 Tablets per Bottle, Rx Only, Boehringer Ingelheim, Roxane Laboratories Inc.,

Schering-Plough Products, LLC recalls Temodar (temozolomide) Capsule, 20 mg per capsule, 5 capsules per package, For Oral Administration, Rx Only, Cytotoxic,

City Versa Strollers Recalled by Baby Jogger Due to Fall Hazard

Wing Enterprises Recalls Switch-it Stepladder/Stepstools Due to Fall Hazard; Sold exclusively at Home Depot

Fu San Machinery Recalls Low Lead Ball Valves Installed in Flammable Gas Lines Due to Fire and Explosion Hazards

Upsher Smith Laboratories, Inc. recalls Divalproex Sodium Delayed-Release Tablets, USP, 500 mg Valproic Acid Activity, 100-count tablets per bottle, Rx only,

Brower Enterprises Inc recalls WOW, Health Enterprises, Dietary Supplement, 30 Caplets, Distributed by: Health Enterprises, 1002 E 5th St., Canton, SD

High-Powered Magnet Sets Recalled by Reiss Innovations Due to Ingestion Hazard; Sold Exclusively on Amazon.com

West-ward Pharmaceutical Corp. recalls Carisoprodol Tablets, USP, 350 mg, packaged in a) 500-count tablets per bottle (NDC 0143-1176-05) and b) 1000-count

Bayer Healthcare, LLC recalls Bronkaid Dual Action Formula, Ephedrine Sulfate 25 mg/Bronchodilator, Guaifenesin 400 mg/Expectorant, a) 24 coated

West-ward Pharmaceutical Corp. recalls Propylthiouracil Tablets, USP, 50 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1480-01) and b) 1000-count

West-ward Pharmaceutical Corp. recalls Lisinopril Tablets, USP 40 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1270-01); b) 1000-count tablets

Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals recalls Hydrocodone bitartrate and acetaminophen Tablets, USP, 10 mg/500 mg, packaged in a) 30-count bottles, NDC 0603-3888-16;

Ridgid Pneumatic Nailers Recalled by One World Technologies Due to Laceration or Injury Hazard; Sold Exclusively at the Home Depot

Grandin Road Recalls Chairs Due to Fall Hazard

Dream On Me Recalls Children's Bed Rails Due to Suffocation and Strangulation Hazards

Dream On Me Recalls Bath Seats Due to Drowning Hazard

Cybex International Recalls Leg Press Due to Risk of Injury

West-ward Pharmaceutical Corp. recalls PredniSONE Tablets, USP, 10 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1473-01), b) 1000-count tablets

West-ward Pharmaceutical Corp. recalls PredniSONE Tablets, USP, 20 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1477-01), b) 500-count tablets

Teva Pharmaceuticals USA, Inc. recalls Copaxone (glatiramer acetate injection), 20 mg/1 mL, packaged in 30 single use PRE-FILLED syringes and 33 Alcohol Preps

Oklahoma Respiratory Care Inc recalls Oxygen, Compressed USP UN1072 Medical Gas supplied in a) 682 litres and b)165 litres cylinders, Rx only, Oklahoma