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
Lupin Pharmaceuticals Inc. recalls Ethambutol Hydrochloride Tablets USP, 400 mg, 100-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals,
Lupin Pharmaceuticals Inc.Feb 22, 2013
⛔ Stop using nowConsumer product
Homelite Recalls Electric Blower Vacuums Due to Laceration Hazard; Sold Exclusively at Home Depot
Homelite recalls electric blower vacuums with specific model/serial numbers due to laceration risk from objects breaking through plastic housing during use. Consumers must stop using and get a refund.
HomeliteFeb 21, 2013
⛔ Stop using nowConsumer product
Electric Blower Vacuums Recalled by OWT Industries Due to Laceration Hazard; Sold Exclusively at Walmart
Expert Gardener electric blower vacuums with specific model and serial numbers recalled due to laceration risk from objects breaking through plastic housing. Consumers must stop using and get a refund.
Expert GardenerFeb 21, 2013
ℹ️ UnratedDrug
Novartis Consumer Health recalls Target Up & Up, athlete's foot cream, full prescription strength, terbinafine hydrochloride 1% antifungal, 30 g (1 oz),
Novartis Consumer HealthFeb 19, 2013
ℹ️ UnratedDrug
Novartis Consumer Health recalls Voltaren Gel (diclofenac sodium topical gel) 1%, for topical use only, RX only, a) Packaged in 20 gm tubes, NDC

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

Latest recalls

Lupin Pharmaceuticals Inc. recalls Ethambutol Hydrochloride Tablets USP, 400 mg, 100-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals,

Homelite Recalls Electric Blower Vacuums Due to Laceration Hazard; Sold Exclusively at Home Depot

Electric Blower Vacuums Recalled by OWT Industries Due to Laceration Hazard; Sold Exclusively at Walmart

Novartis Consumer Health recalls Target Up & Up, athlete's foot cream, full prescription strength, terbinafine hydrochloride 1% antifungal, 30 g (1 oz),

Novartis Consumer Health recalls Voltaren Gel (diclofenac sodium topical gel) 1%, for topical use only, RX only, a) Packaged in 20 gm tubes, NDC

Novartis Consumer Health recalls Lamisil AT Cream (terbinafine hydrochloride 1% antifungal), 12 gm ( .42 oz) Tubes and 30 gm (1 oz) Tubes packaged in

Novartis Consumer Health recalls Novartis Lamisil AT Cream for Jock Itch (terbinafine hydrochloride 1% antifungal), a) 12 g (.42 oz) Tube, NDC

Novartis Consumer Health recalls Novartis Lamisil AT Cream, Terbinafine Hydrochloride Cream 1% Antifungal, Novartis Consumer Health, Inc., Parsippany,

L. Perrigo Co. recalls PE Daytime Cold/Flu LiqGel, Multi Symptom Relief, Acetaminophen/Dextromethorphan HBr/Phenylephrine HCL 325/10/5 mg gel

Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, 50 mL, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7984-36

Warner Chilcott Company LLC recalls Jevantique (norethindrone acetate and ethinyl estradiol) tablets; 1.0 mg/5.0 mcg, 90 count bottle (NDC# 52544-237-19),

Warner Chilcott Company LLC recalls Femhrt (norethindrone acetate and ethinyl estradiol) tablets, 0.5 mg/2.5 mcg, 90 count bottle (NDC#: 0430-0145-23), Rx

Hospira Inc. recalls METRONIDazole Injection, USP 500 mg (5 mg/mL), 100 mL Bag, Rx only, Hospira, Inc. Lake Forest, IL 60045 (NDC

Warner Chilcott Company LLC recalls Femhrt (norethindrone acetate and ethinyl estradiol) tablets, 1.0 mg/5.0 mcg, 90 count bottle ( NDC#: 0430-0544-23), Rx

Dr Reddys Laboratories Tennessee LLC recalls Amoxicillin for Oral Suspension, 125mg/5mL, a) 80 mL (NDC 43598-222-80); b) 100mL, (NDC 43598-222-52); c)150 mL (NDC

John Deere Recalls Gator Utility Vehicles Due to Fire Hazard

Cramer Recalls Folding Step Stools Due to Fall Hazard

Watson Laboratories Inc recalls ZARAH¿ Drospirenone/ Ethinyl Estradiol Tablets, 3.0 mg/0.03 mg, Rx only, 3 tablet dispensers, 28 tablets each, Manuf.

Actavis Elizabeth LLC recalls Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate

Glenmark Generics Inc., USA recalls Montelukast Sodium Tablets, 10 mg (base), packaged in a) 30-count tablets per bottle (NDC 68462-392-30) and b) 90-count

Purr-Fection Stuffed Animals with Flashlights Recalled by MJC Due to Laceration Hazard, Sold Exclusively at Cabela's

Hospira Inc. recalls 0.9% Sodium Chloride Irrigation, USP, 3000 mL, Sterile, Non pyrogenic, Rx Only, Hospira, Inc., Lake Forest, IL 60045,

OLAAX International recalls MAXILOSS Weight Advanced, 225 mg proprietary blend of herbs, supplied in 36 count capsules in Green & Blue Boxes,

Samsonite Recalls Dual-Wattage Travel Converter Kits Due to Fire, Burn Hazards

Bohning Recalls Hunting Crossbows Due to Injury Hazard; Can Fire Unexpectedly

Jubilant Cadista Pharmaceuticals Inc. recalls Pantoprazole Sodium Delayed Release Tablets USP, 40 mg, 90 count bottles, Manufactured by Jubilant Life Sciences Ltd,

Watson Laboratories Inc recalls Meprobamate; Tablets USP, 400 mg, 100 tablets; Rx only; Manufactured By: Watson Laboratories, Inc., Corona, CA 92800

Watson Laboratories Inc recalls Meprobamate, Tablets USP, 200 mg, 100 tablets; Rx only; Manufactured By: Watson Laboratories, Inc., Corona, CA 92800

Teva Pharmaceuticals USA, Inc. recalls CLONAZEPAM ORALLY DISINTERGRATING Tablets, USP, 0.5 mg, 60 tablets (10 blister cards of 6 tablets each), TEVA

Mutsy USA Recalls EVO Strollers Due to Strangulation Hazard