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
Regency Seating Recalls Oakmont Fabric Stackable Chair Due to Fall Hazard; Sold Exclusively by Global Industrial Equipment
Regency recalls Oakmont fabric stackable chairs sold by Global Industrial Equipment due to risk of leg weld breaking and causing falls. Consumers must stop using and get a free replacement.
RegencyMar 5, 2013
⛔ Stop using nowConsumer product
Disco Lights Recalled by Tween Brands Due to Electrical Shock Hazard; Sold Exclusively at Justice
Tween Brands disco lamps (styles 90052: black, 901651: star) sold at Justice stores recalled due to electrical shock risk from accessible wiring. Return for full refund.
Tween BrandsMar 5, 2013
⛔ Stop using nowConsumer product
Briggs & Stratton Recalls Ariens Compact Snow Blowers Due to Fire Hazard
Briggs & Stratton recalls Ariens Compact Snow Blowers with model 920014 and serial numbers 100,000-119,039 due to fire risk from gas escaping the carburetor bowl nut. Consumers must stop using and return for repair.
Briggs & StrattonMar 5, 2013
ℹ️ UnratedDrug
CareFusion 213, LLC recalls Blood Culture Prep Kit II containing 1 FREPP (70% isopropyl alcohol), Net 1.1 mL and 1 SEPP (iodine tincture 2% USP),
CareFusion 213, LLCMar 4, 2013

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

Latest recalls

Regency Seating Recalls Oakmont Fabric Stackable Chair Due to Fall Hazard; Sold Exclusively by Global Industrial Equipment

Disco Lights Recalled by Tween Brands Due to Electrical Shock Hazard; Sold Exclusively at Justice

Briggs & Stratton Recalls Ariens Compact Snow Blowers Due to Fire Hazard

CareFusion 213, LLC recalls Blood Culture Prep Kit II containing 1 FREPP (70% isopropyl alcohol), Net 1.1 mL and 1 SEPP (iodine tincture 2% USP),

CareFusion 213, LLC recalls SEPP 2% Iodine Tincture USP (47% v/v Ethyl Alcohol, 2% w/v Iodine, USP, Sodium Iodide USP, & Purified Water USP),

CareFusion 213, LLC recalls FREPP/SEPP Kit containing 1 FREPP (povidone iodine 2% aqueous solution), Net 1.1 mL and 1 SEPP (povidone iodine 10%

CareFusion 213, LLC recalls SEPP 70% Isopropanol (isopropyl alcohol) 70% v/v, USP, 200-count applicators (net 0.67 mL each) per carton, Cat. No

CareFusion 213, LLC recalls Donor Prep Kit containing 1 FREPP (70% isopropyl alcohol), Net 1.1 mL and 1 SEPP (iodine tincture 2% USP), Net 0.67 mL

CareFusion 213, LLC recalls SEPP 10% Povidone Iodine Solution USP (1% available Iodine, Surfactant & USP Purified Water), packaged in a) 200-count

Physicians Total Care, Inc. recalls Voltaren 1% Gel, 100 gm tube, Rx only, Dist By: Physicians Total Care, Tulsa OK 74146, Mfg By: Novartis Consumer

SlumberWorld Recalls Mattresses Due to Violation of Federal Mattress Flammability Standard

Balsam Hill Recalls Pre-lit Christmas Trees Due to Burn and Shock Hazards

Baxter Healthcare Corp. recalls 0.9% Sodium Chloride Injection, USP, 50 mL Mini-Bag Plus Container, Rx only, distributed by Baxter Healthcare

Mutual Pharmaceutical Company, Inc. recalls Fenofibric Acid, immediate release tablet, 35 mg, 30 count bottle Rx only, Mutual Pharmaceutical Co., Inc.,

Mutual Pharmaceutical Company, Inc. recalls FIBRICOR (fenofibric acid) Tablets, 105 mg, a) 30 count bottle (NDC 13310-102-07), b) 90 count bottle (NDC

Mutual Pharmaceutical Company, Inc. recalls Fenofibric Acid, immediate release tablet, 105 mg, a) 30 count bottle (NDC 53489-678-07), b) 90 count bottle (NDC

Liberty Mountain Recalls Mountain Climbing Lanyards Due to Risk of Serious Injury

Jerdon Style Recalls One-Cup Coffeemakers Due to Burn and Fire Hazards

Hospira Inc. recalls Sodium Acetate Injection, USP, 40 mEq/20 ml (2 mEq/mL) 20 mL Single-Dose Fliptop, Rx only, HOSPIRA, INC. LAKE FOREST,

Teva Pharmaceuticals USA, Inc. recalls Cefdinir for Oral Suspension, 125 mg/5 mL, packaged in a) 60 mL bottle (NDC 0093-4136-64); b) 100 mL bottle (NDC

Sanofi-Synthelabo recalls Rifadin (rifampin) capsules, USP, 150 mg, 100-count capsules per bottle, Manufactured by: Fabrique par Sanofi-Aventis

Mylan Pharmaceuticals Inc. recalls Lisinopril Tablets, USP 10 mg, Rx only, 1000 count bottles, Manufactured for: Mylan Pharmaceuticals Inc ,Morgantown, WV

Hospira Inc. recalls QUELICIN (succinylcholine chloride) Injection, USP, 200 mg (20 mg/mL) 10 mL, Rx only, HOSPIRA, INC. LAKE FOREST, IL

Hospira Inc. recalls Furosemide Injection, USP, 40 mg/4mL (10 mg/mL), 4 ml Single-Dose Vial, Rx only, HOSPIRA, INC. LAKE FOREST, IL 60045

Hospira Inc. recalls Diazepam Injection, USP 5 mg/mL, 10 mL, Multiple-dose fliptop vial, RX only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA,

One World Technologies Recalls Ryobi Cordless Tool Battery Pack Due to Fire and Burn Hazards

Dynacraft Recalls Monster High City Motor Scooters Due to Fall Hazard; Sold Exclusively at Walmart

Dynacraft Recalls Hello Kitty City Motor Scooters Due to Fall Hazard; Sold Exclusively at Toys R Us

Hospira Inc. recalls Propofol Injectable Emulsion, 1%, packaged in a) 5 x 20 mL Single patient infusion vials per carton, 200 mg/20 mL (10

Petnet Solution Inc recalls Fludeoxyglucose F 18 Injection USP, 20-200 mCi/mL, Diagnostic - For Intravenous Use Only, Manufactured by PETNET