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FDA Medical Device Recalls

View 10000 FDA Medical Device Recalls on BEUDAMED, the Better Database on Medical Devices. This searchable listing aggregates recall notices issued by the U.S. Food and Drug Administration for devices removed, corrected, or returned due to safety, labeling, or performance concerns. Each record summarizes the recall reason, affected models and lots, recall class, and recommended actions for patients and providers.

Searchable filters help stakeholders identify affected manufacturers, device models, and recall classes (Class I–III) and review timelines and remediation steps. Healthcare providers and purchasers can use these records to verify whether inventory is affected and to implement recommended corrections, returns, or patient notifications.

Victory Motorized Vehicle, 3 wheel Model SC1600

FDA Recall
Terminated ·Pride Mobility Product Corp·Product code INI·July 1, 2004

Victory Motorized Vehicle 4 wheels Model SC1700

FDA Recall
Terminated ·Pride Mobility Product Corp·Product code INI·July 1, 2004

LeMaitre Embolectomy Catheter 2F Single Lumen, Balloon Volume 0.05 ml , Length 80 cm Latex Product Number: 1601-28

FDA Recall
Terminated ·Lemaitre Vascular, Inc.·Product code DXE·February 7, 2005

Patient tables of CT systems with brand name: CT/e; CT/e Dual; CT/e Plus, CT/e Dual Plus; CT/e Lite; ProSpeed AI; ProSpeed AII; ProSpeed FI; ProSpeed FII; ProSpeed EII; CT HiSpeed Series.

FDA Recall
Terminated ·General Electric Med Systems LLC·Product code IXR·October 21, 2004

Zimmer Orthopaedic Surgical Products, Disposable Cuff, Single Port, Double Bladder Cuff, Sterile, Zimmer, Dover, OH USA. The cuff is a sterile, single use product equipped with an integral fill line. The product is packed 10 cuffs per unit.

FDA Recall
Terminated ·Zimmer Orthopaedic Surgical Products·Product code KCY·February 11, 2005

Flexiflo Quantum Enteral Pump

FDA Recall
Terminated ·Ross Products Division Abbott Laboratories·Product code LZH·August 18, 2004

Charger Assembly, Model # SC-5300, of the PRECISION Spinal Cord Stimulation System

FDA Recall
Terminated ·Advanced Bionics Corporation·Product code LGW·November 11, 2004

METRx II Tube, 20mm x 6cm stainless steel tubular retractor, Part No. 9569723

FDA Recall
Terminated ·Medtronic Sofamor Danek Instrument Manufacturing·Product code LXH·January 25, 2006

METRx II Tube, 14mm x 5cm stainless steel tubular retractor, Part No. 9569662

FDA Recall
Terminated ·Medtronic Sofamor Danek Instrument Manufacturing·Product code LXH·January 25, 2006

Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line Reinforcement. Do not reuse. Ethylene Oxide Sterilized. Made in the U.S.A. Synovis Surgical Innovations A division of Synovis Life Technologies, Inc., 2575 University Ave. W., St. Paul, MN 55114-1024 USA.

FDA Recall
Terminated ·Synovis Surgical Inovation Div. of·Product code FTM·November 1, 2005