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

77,052 found

✓ Lower riskMedical device
Boston Scientific Corporation recalls ACCOLADE DR Pacemaker, SL (Model Number L301), SL MRI (Model Number L311), EL (Model Number L321), and EL MRI (Model
Boston Scientific is a leading global medical device company specializing in cardiovascular, neurovascular, and endovascular solutions. We provide innovative products for the treatment of heart disease, stroke, and other conditions.
Boston ScientificDec 12, 2024
✓ Lower riskMedical device
Boston Scientific Corporation recalls VALITUDE CRT-P, EL (Model Number U125) and EL MRI (Model Number U128)
Boston Scientific is a global leader in medical devices, providing innovative solutions for cardiovascular, neurovascular, and other medical specialties.
Boston ScientificDec 12, 2024
✓ Lower riskMedical device
Medtronic Perfusion Systems recalls DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014 (14 Fr)
Medtronic recalls specific pediatric arterial cannula models due to incorrect labeling in certain lots. Affected units may have labeling errors that could lead to improper use during medical procedures.
Medtronic Perfusion SystemsDec 12, 2024
⚠️ Use cautionMedical device
Abiomed, Inc. recalls Impella RP Flex with SmartAssist; Product Number: 1000323;
Abiomed recalls Impella RP Flex with SmartAssist pumps with serial numbers listed. Optical sensors may be damaged during insertion or manipulation of guidewires or central venous lines, causing temporary or permanent pump stop. Check your pump's serial number against the list.
AbiomedDec 12, 2024

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

Latest recalls

Boston Scientific Corporation recalls ACCOLADE DR Pacemaker, SL (Model Number L301), SL MRI (Model Number L311), EL (Model Number L321), and EL MRI (Model

Boston Scientific Corporation recalls VALITUDE CRT-P, EL (Model Number U125) and EL MRI (Model Number U128)

Medtronic Perfusion Systems recalls DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014 (14 Fr)

Abiomed, Inc. recalls Impella RP Flex with SmartAssist; Product Number: 1000323;

LivaNova USA, Inc. recalls SenTiva, REF: 1000C, Generators Part of the VNS Therapy System with Microburst Stimulation. Used for Vagus Nerve

LivaNova USA, Inc. recalls SenTiva, REF: 1000; SenTiva Duo, REF: 1000-D; Generators Part of the VNS Therapy System. Used for Vagus Nerve

Boston Scientific Corporation recalls PROPONENT DR Pacemaker, SL (Model Number L201), (VDD) SL (Model Number L209), SL MRI (Model Number L211), EL (Model

GNMart LLC recalls FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles

Akron Pharma, Inc. recalls Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., 373 US

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

Akron Pharma, Inc. recalls Diphenhydramine HCl 25 mg, 100 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., 373 RT US 46 W

Akron Pharma, Inc. recalls Acetaminophen Regular Strength, 325 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite

Ascend Laboratories, LLC recalls Dabigatran Etexilate, 75 mg capsules, 60-count bottles, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA,

Ascend Laboratories, LLC recalls Dabigatran Etexilate, 150mg capsules, 60-count bottles, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA,

Buy-Herbal recalls Nhan Sam Tuyet Lien Truy Phong Hoan, Capsules, 30-Count Bottles, Manufactured by Yee Hong Pharmaceuticals, SDN, Penang,

Akron Pharma, Inc. recalls Diphenhydramine HCl 50 mg, 1000 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc. 373 Route US

Akron Pharma, Inc. recalls Diphenhydramine HCl 25 mg, 1000 Capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., 373 RT US 46 W

Akron Pharma, Inc. recalls Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ

WHOLESALE PRODUCE SUPPLY LLC DBA recalls Cucumbers, Wholesale Produce Supply, 752 Kasota Circle, Minneapolis, MN 554145. Product of Mexico. Cucumbers sold in

COREPACK MANUFACTURING INC recalls White Maeng da, kratom powder product packaged mylar resealable bags. 3 oz package, 80 bags per shipper box.

Shata Traders Inc. recalls THREE RIVERS brand TUTTI-FRUTTI; INGREDIENTS Papaya Cubes, Sugar, Citric Acid (E-330), Potassium Sorbate (E-202), FD&C

Yoto Reannounces Recall of Yoto Mini Speakers for Children Due to Burn and Fire Hazards; New Full Battery Replacement Kit Now Available

Touch of Class® Recalls Wall Teester Bed Crowns Due to Injury Hazard

Stanley Recalls 2.6 Million Switchback and Trigger Action Travel Mugs Due to Burn Hazard

Mr. Christmas Recalls Wireless Decorative Tree Light Controllers Due to Fire Hazard

HTRC C240 Battery Chargers Recalled Due to Fire and Burn Hazards; Risk of Serious Injury and Death; Manufactured by Shenzhen Haitan Technology Co.

BMW X3 (2025) recall — Air Bags

HF Acquisition Co LLC recalls Biological, Bio52 HealthFirst Mail In Monitoring System, 52 Tests, Item: 1003600. Biological, Bio12 HealthFirst Mail In

MICROVENTION INC. recalls MicoVention Terumo, LVIS Intraluminal Support Device, REF: 213522-CAS, od, 3.5 mm, TL 22 mm, WL 18 mm, Sterile R,

Nuwellis Inc recalls nuwellis AquaFlexFlow UF 500 Plus, REF 114156, Catalog Number A06163, extracorporeal blood circuit which is used with