Medical Device Recalls
This is our largest category by volume. The FDA tracks recalls for an enormous range of medical devices: implants, pacemakers, insulin pumps, surgical tools, blood glucose monitors, X-ray machines, prosthetics, contact lenses, and home health equipment, among many others. We have records dating back to 2005 and add new ones as the FDA publishes them.
Device recalls can happen because of software bugs, manufacturing defects, bacterial contamination, incorrect labeling, or design flaws that lead to inaccurate results or equipment failure. Class I recalls are the most serious and mean the device could cause injury or death.
Showing 2741–2760 of 38,428 recalls
Recalled Item: remel BLOOD AGAR EMB AGAR BIPLATE
The Issue: Listeria Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: remel BLOOD AGAR MacCONKEY AGAR BIPLATE
The Issue: Listeria Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: namic convenience kits labeled as: 1) MTS
The Issue: The female luer fittings on the Pressure Monitoring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: namic convenience kits labeled as: PML
The Issue: The female luer fittings on the Pressure Monitoring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: namic convenience kits labeled as: MTS
The Issue: The female luer fittings on the Pressure Monitoring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: namic convenience kits labeled as: KIT
The Issue: The female luer fittings on the Pressure Monitoring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zebra Thermal Barcode Printer GX430t
The Issue: Power supply unit for Zebra Printers used with
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z1 Femoral Hip System
The Issue: There is a potential design issue with the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL TB Stain Kit K
The Issue: One component of the kit was shipped with
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) C SCOPE DISPOSABLE KIT
The Issue: Medical convenience kits contain plastic syringes affected by
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) AV FISTULA PACK-LF
The Issue: Medical convenience kits contain plastic syringes affected by
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) ANGIOGRAPHY SPECIALS
The Issue: Medical convenience kits contain plastic syringes affected by
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) LACERATION TRAY
The Issue: Medical convenience kits contain plastic syringes affected by
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) ACOUSTIC NEUROMA PACK-LF
The Issue: Medical convenience kits contain plastic syringes affected by
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) ABLATION PACK
The Issue: Medical convenience kits contain plastic syringes affected by
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) BILLINGS CLINIC SC HEAD & NECK
The Issue: Medical convenience kits contain plastic syringes affected by
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) CV NEONATAL PACK
The Issue: Medical convenience kits contain plastic syringes affected by
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) BILATERAL FACET TRAY
The Issue: Medical convenience kits contain plastic syringes affected by
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) AV FISTULA PACK
The Issue: Medical convenience kits contain plastic syringes affected by
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) CLOVIS ROBOTIC-LF
The Issue: Medical convenience kits contain plastic syringes affected by
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.