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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.

Sensi-Touch Pediatric Lumbar Puncture Tray with Safety Components 22G X2.5 inch Product Number: 8888714113

FDA Recall
Terminated ·Kendall Healthcare Products Co·Product code FMI·October 8, 2004

Kendall MONOJECT MAGELLAN 3cc Syringe with Safety Needle 22G X 1.5 inch Product Number: 5551833215

FDA Recall
Terminated ·Kendall Healthcare Products Co·Product code FMI·October 8, 2004

Kendall MONOJECT MAGELLAN SAFETY NEEDLE 21G X 1 inch Product Number: 8881850110

FDA Recall
Terminated ·Kendall Healthcare Products Co·Product code FMI·October 8, 2004

Curity Adult Lumbar Puncture Tray with Safety Components 20G x 3.5 inch Product Code: 1032

FDA Recall
Terminated ·Kendall Healthcare Products Co·Product code FMI·October 8, 2004

Goldenberg Snarecoil Bone Marrow Biopsy / Aspiration Tray with Safety Components, 16G x 5 inch Bone Marrow needle plus ''I'' type Sternal / Iliac needle Product Number: SC4508

FDA Recall
Terminated ·Kendall Healthcare Products Co·Product code FMI·October 8, 2004

Oral-B CrossAction PowerMAX Rechargeable Toothbrush, , Soft 4 Accent Colors: Blue, Pink, Green. Purple NDC 0-69055-83293-6

FDA Recall
Terminated ·Gillette Research Institute·Product code JEQ·October 27, 2004

Kendall MONOJECT MAGELLAN 3cc Syringe with Safety Needle 21G X 1 inch Product Number: 5551833110

FDA Recall
Terminated ·Kendall Healthcare Products Co·Product code FMI·October 8, 2004

Ultra Power Burs, Sterile, Single-Use.

FDA Recall
Terminated ·Linvatec Corp.·Product code HRX·August 26, 2004

Stryker Navigation System - Hip Module Patient Tracker, green; Model 6007-005-000.

FDA Recall
Terminated ·Stryker Instruments, Instruments Div.·Product code HAW·July 14, 2004

BD Vacutainer Microtainer Serum tubes (with or without gel).

FDA Recall
Terminated ·Becton Dickinson & Company·Product code JKA·August 20, 2004