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

⚠️ Use cautionMedical device
Orthoscan, Inc. recalls Ziehm Vision FD. Interventional fluoroscopic x-ray system
Orthoscan recalls Ziehm Vision FD interventional fluoroscopy systems with serial numbers 93412-93662. Defective hand switches could cause unintended X-ray radiation if dropped or impacted.
Ziehm VisionAug 8, 2024
⚠️ Use cautionMedical device
Orthoscan, Inc. recalls Ziehm Vision RFD 3D. Interventinoal fluoroscopic x-ray system
Orthoscan recalls Ziehm Vision RFD 3D fluoroscopy systems with serial numbers listed. Defective hand switches could cause unintended X-ray radiation if dropped or impacted.
Ziehm VisionAug 8, 2024
✓ Lower riskMedical device
Fresenius Medical Care Holdings, Inc. recalls Blood Pressure Module BPM3 TM-2917B (Spare Part Numbers 191378 or 191389) with firmware version S005 installed in 2008
Fresenius Medical Care is a leading global provider of medical devices and healthcare solutions, including dialysis machines, infusion systems, and more.
Fresenius Medical CareAug 8, 2024
⚠️ Use cautionMedical device
Orthoscan, Inc. recalls Ziehm Vision R. Iterventional fluoroscopic x-ray system
Orthoscan recalls Ziehm Vision R interventional fluoroscopy systems due to potential unintended X-ray radiation from faulty hand switches after drops or impacts.
Ziehm VisionAug 8, 2024
⚠️ Use cautionMedical device
Orthoscan, Inc. recalls Ziehm Vision system, x-ray, tomography, computed.

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

Latest recalls

Orthoscan, Inc. recalls Ziehm Vision FD. Interventional fluoroscopic x-ray system

Orthoscan, Inc. recalls Ziehm Vision RFD 3D. Interventinoal fluoroscopic x-ray system

Fresenius Medical Care Holdings, Inc. recalls Blood Pressure Module BPM3 TM-2917B (Spare Part Numbers 191378 or 191389) with firmware version S005 installed in 2008

Orthoscan, Inc. recalls Ziehm Vision R. Iterventional fluoroscopic x-ray system

Orthoscan, Inc. recalls Ziehm Vision system, x-ray, tomography, computed.

T.G. Eakin Limited recalls eakin Cohesive seal, small, Model Number 839002, ostomy barrier seal

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

GE Healthcare GmbH recalls ViewPoint 6, Model Numbers: a) H47581RJ, b) H47591MA, c) H47591MT, d) H47591PE, e) H47591PR, f) H47591RA, g) H47591SD,

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

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Allura Xper systems (R8.1 with Poly-G Stand) Interventional Fluoroscopic X-Ray System, Model Numbers 722010,

Alcon Research LLC recalls DAILIES TOTAL1, DAILIES TOTAL1 for Astigmatism, DAILIES TOTAL1 Multifocal, TOTAL30 Sphere,

Orthoscan, Inc. recalls Ziehm Vision RFD. Interventional fluoroscopic x-ray system

Orthoscan, Inc. recalls Ziehm Solo FD. Interventional fluoroscopic x-ray system

Orthoscan, Inc. recalls Ziehm Solo. Digital Mobile C-arm

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

Zimmer GmbH recalls Biolox Option Taper Sleeve, Type 1 Taper, -6mm Neck - Indicated for use in total hip replacement with cemented or

Preferred Pharmaceuticals, Inc. recalls Ibuprofen Tablets, USP 400mg, Generic for Motrin, Pkg Size: 30 tablets per bottle, Mfg: Dr. Reddy's Laboratories,

Teva Pharmaceuticals USA, Inc recalls Testosterone Gel, 1.62%, (Alcohol 80% v/v), 30 unit-dose packets, Rx Only, Teva Pharmaceuticals, USA, Inc. North Wales,

Kester Foods LLC recalls Yummy Monkey Organics Real Movie Theater Popcorn, Made With Purified Ghee & Himalayan Sea Salt. UPC 9 96692 66654 2,

Kester Foods LLC recalls Yummy Monkey Organics Butter & Yeast Popcorn, Made With Purified Ghee & Nutritional Yeast. UPC 9 96692 66641 2,

SMEG USA Recalls Refrigerators Due to Injury Hazard

Samsung Recalls Slide-In Electric Ranges Due to Fire Hazard

Chem-Pak Recalls Finger-Ease Guitar String Lubricants Due to Skin Irritation Hazard

NOVA BUS LFS (2023) recall — Parking Brake

NOVA BUS LFS (2023) recall — Visibility

JEEP CHEROKEE (2021) recall — Air Bags

American Contract Systems, Inc. recalls Open Shoulder, LWOS39L; Medical convenience kit

Cook Biotech, Inc. recalls Biodesign Fistula Plug C-FPS-0.4 - For implantation to reinforce soft tissue for repair of recto-vaginal or anorectal

American Contract Systems, Inc. recalls Arthroscopy Pack, MSKA45A; Medical convenience kit

Cook Biotech, Inc. recalls Biodesign Fistula Plug C-FPS-0.7 - For implantation to reinforce soft tissue for repair of recto-vaginal or anorectal