SEO landing

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.

Smiths Medical CADD-Sentry Pro Medication Safety Software - electronic pump protocol programming software - Administrator REF 21-6275-51 RX only, Smiths Medical MD, Inc. St Paul, Minnesota 55112 USA

FDA Recall
Terminated ·Smiths Medical MD, Inc.·Product code FRN·August 14, 2007

TENET Medical Engineering Wrist Stabilization Kit, Medium; REF (Part) #7692; Sterile; manufactured by TENET Medical Engineering, Calgary, Alberta, Canada T2Z 4M3.

FDA Recall
Terminated ·Tenet Medical Engineering Inc 11979 40th St Se /#203 Ab Calgary Canada·Product code JEB·November 23, 2007

Size 8 Pedicle Screws of the Allez Spine Laguna Pedicle Screw System, Screw Size (diameter x length) 8 x 55, Catalog Number LG-PR0855, Allez Spine, LLC., Irvine, CA

FDA Recall
Terminated ·Allez Spine, LLC·Product code MNI·July 30, 2007

Size 8 Pedicle Screws of the Allez Spine Laguna Pedicle Screw System, Screw Size (diameter x length) 8 x 80, Catalog Number LG-PR0880, Allez Spine, LLC., Irvine, CA

FDA Recall
Terminated ·Allez Spine, LLC·Product code MNI·July 30, 2007

Smith & Nephew, Inc., Exu-Dry Wound Burn Dressing, Product Number: 5999L74, Exu-Dry Sheet 36"x72" Permeable with Straps Quilted, Smith & Nephew, Inc.,Largo, Florida.

FDA Recall
Terminated ·Smith And Nephew, Inc. Wound Management Division·Product code MCY·November 21, 2007

Smith & Nephew, Inc., Exu-Dry Wound Burn Dressing, Product Number: 5999018, Exu-Dry Dressing, 15" x 18", Smith & Nephew, Inc.,Largo, Florida.

FDA Recall
Terminated ·Smith And Nephew, Inc. Wound Management Division·Product code MCY·November 21, 2007

Smith & Nephew, Inc., Exu-Dry Wound Burn Dressing, Product Number: 5999LV1, Exu-Dry Large Burn Vest, Smith & Nephew, Inc.,Largo, Florida

FDA Recall
Terminated ·Smith And Nephew, Inc. Wound Management Division·Product code MCY·November 21, 2007

Size 8 Pedicle Screws of the Allez Spine Laguna Pedicle Screw System, Screw Size (diameter x length) 8 x 45, Catalog Number LG-PR0845, Allez Spine, LLC., Irvine, CA

FDA Recall
Terminated ·Allez Spine, LLC·Product code MNI·July 30, 2007

Abbott, ACCELERATOR Device Manager (ADM); List Number: 08H74-01; Abbott Laboratories, Abbott Park, IL

FDA Recall
Terminated ·Abbott Laboratories, Inc·Product code JQP·October 25, 2007

Depuy TK2 Compression Hip Screw trauma plate, Short Barrel, 135 DEG, 4H-92.6mm, sterile; REF 8315-35-104, DePuy Orthopaedics, Inc., Warsaw, IN 46581

FDA Recall
Terminated ·Depuy Orthopaedics, Inc.·Product code KTT·October 30, 2007