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

77,053 found

✓ Lower riskMedical device
Olympus Corporation of the Americas recalls Soltive Pro SuperPulsed Laser Systems-Intended for incision, excision, resection, ablation, coagulation, hemostasis,
Olymp: Soltive Pro SuperPulsed Laser Systems may display 'Kidney Stone' instead of 'Bladder Stone' in Spanish/Portuguese, risking incorrect energy delivery during procedures.
OlympusAug 13, 2024
✓ Lower riskMedical device
Zoe Medical Incorporated recalls Spacelabs Ultraview DM4 Vital Signs Monitor (all variations -M, -N, -MF, -NF, -MW, -NW, -MFW, -NFW), Model Number 91331
Zoe Medical recalls Spacelabs Ultraview DM4 Vital Signs Monitors with outdated battery warnings. All model variations and serial numbers up to GFD10486 are affected. This labeling issue may lead to risks from damaged or expired batteries.
Zoe MedicalAug 13, 2024
✓ Lower riskMedical device
Olympus Corporation of the Americas recalls Soltive Premium SuperPulsed Laser - Intended for incision, excision, resection, ablation, coagulation, hemostasis, and
Olympus recalls Soltive Premium SuperPulsed Laser due to incorrect Spanish/Portuguese translation of 'Bladder Stone' as 'Kidney Stone' on the GUI, potentially causing incorrect energy delivery during procedures.
OlympusAug 13, 2024
✓ Lower riskMedical device
Zoe Medical Incorporated recalls Spacelabs Ultraview DM3 Vital Signs Monitor (all variations -M, -MT, -N, -NT), Model Number 91330
Zoe Medical recalls Spacelabs Ultraview DM3 Vital Signs Monitors with model 91330 due to inadequate battery safety warnings. Owners should check serial numbers up to FFD8292 for affected units.
Zoe Medical

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

Latest recalls

Olympus Corporation of the Americas recalls Soltive Pro SuperPulsed Laser Systems-Intended for incision, excision, resection, ablation, coagulation, hemostasis,

Zoe Medical Incorporated recalls Spacelabs Ultraview DM4 Vital Signs Monitor (all variations -M, -N, -MF, -NF, -MW, -NW, -MFW, -NFW), Model Number 91331

Olympus Corporation of the Americas recalls Soltive Premium SuperPulsed Laser - Intended for incision, excision, resection, ablation, coagulation, hemostasis, and

Zoe Medical Incorporated recalls Spacelabs Ultraview DM3 Vital Signs Monitor (all variations -M, -MT, -N, -NT), Model Number 91330

Smith & Nephew Inc. recalls ROTATION MEDICAL TENDON STAPLES (8) (broad indication)-Intended for fixation of prosthetic material to soft tissues.

Merit Medical Systems, Inc. recalls Prelude Sheath Introducer 7.5F, REF: PSI-7F-11-038 Version F (PSI-7F-11-038/F)

Becton, Dickinson and Company, BD Bio Sciences recalls BD FACSDuet Premium Sample Preparation System, REF: 666340, 666339; and BD FACSDuet Sample Preparation System (Base),

SEER MEDICAL PTY LTD recalls Seer Home System is an ambulatory electroencephalograph (EEG) system intended for at-home use for extended EEG and

Smith & Nephew Inc. recalls ROTATION MEDICAL TENDON STAPLES (8) (narrow indication)-Intended for fixation of prosthetic material to soft tissues.

Merit Medical Systems, Inc. recalls Custom Procedure Kit, REF: K12T-11077

FDC Limited recalls Timolol Maleate Ophthalmic Solution USP, 0.5%, packaged in: a) 5mL bottle (NDC 64980-514-05), and b) 10mL bottle (NDC

Flagstone Foods, LLC recalls 6.5oz Emerald Kettle Glazed Walnut, UPC: 0 10300 80894 7

FORD ESCAPE (2024) recall — Electrical System

FOREST RIVER IMPRESSION (2021) recall — Equipment

FOREST RIVER GEORGETOWN (2025) recall — Equipment

FORD EXPLORER (2025) recall — Equipment

Wipro GE Healthcare Private Ltd. recalls GE Giraffe Warmer, Model/Catalog Number M1118179-01090979. Infant radiant warmers provide infrared heat in a controlled

Physio-Control, Inc. recalls STERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP20 STERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP15

Wipro GE Healthcare Private Ltd. recalls GE Panda iRES Warmer, Model/Catalog Numbers: 1) M1112198-01045518; 2) M1112198-01045579; 3) M1112198-01047148; 4)

Murata Vios, Inc. recalls Vios Monitoring System Bedside Monitor Model BSM2050

Direct Rx recalls Ibuprofen 800mg, Generic for: Motrin, Each tablet contains: Ibuprofen, USP 800 mg, Packaged and Distributed by: DIRECT

Prime Food Processing Corp. recalls Prime Food brand Steam Bun with Egg Custard Added; 10pcs/pack; NET WT. 20 oz (1lb.4 oz) 568g; KEEP FROZEN; INGREDIENTS:

Prime Food Processing Corp. recalls Prime Food brand Steam Bun with Egg Custard & Coconut Added; 10pcs/pack; NET WT. 20 oz (1lb.4 oz) 568g; KEEP FROZEN;

JEEP GRAND CHEROKEE (2024) recall — Child Seat

CADILLAC LYRIQ (2023) recall — Service Brakes, Hydraulic

GE Healthcare GmbH recalls ViewPoint; system, imaging processing, radiological

Zimmer GmbH recalls Biolox Option Taper Sleeve, Type 1 Taper, Standard Neck - Indicated for use in total hip replacement with cemented or

Epilog Laser Corp. recalls Fusion Pro 24, Model 17000

Datascope Corp. recalls CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP (IABP). Electromechanical system used to inflate and deflate intra-aortic

B. Braun Medical, Inc. recalls AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual Manifold, Four-way Stopcock, Model/Catalog