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 36721–36740 of 38,428 recalls
Recalled Item: Persona
The Issue: All lots of the Persona Cemented Tibial Drill,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona
The Issue: All lots of the Persona Cemented Tibial Drill,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona
The Issue: All lots of the Persona Cemented Tibial Drill,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona The Personalized Knee System
The Issue: All lots of the Persona Cemented Tibial Drill,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona
The Issue: All lots of the Persona Cemented Tibial Drill,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona
The Issue: All lots of the Persona Cemented Tibial Drill,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona
The Issue: All lots of the Persona Cemented Tibial Drill,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona The Personalized Knee System
The Issue: All lots of the Persona Cemented Tibial Drill,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona
The Issue: All lots of the Persona Cemented Tibial Drill,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona The Personalized Knee System
The Issue: All lots of the Persona Cemented Tibial Drill,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novocastra Ready-to-Use Mouse Monoclonal Antibody Terminal Deoxynuceotidyl...
The Issue: RTU-TdT-339 is not stable up to the expiry
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare ADVIA Centaur Digitoxin (DGTN) 250 Test 09046419 50
The Issue: Operating range of the ADVIA Centaur systems is
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare ADVIA Centaur CA 19-9 250 Test 10491244 50
The Issue: Operating range of the ADVIA Centaur systems is
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare ADVIA Centaur DHEA-504 (DHEAS) 50 Test 06489701 The
The Issue: Operating range of the ADVIA Centaur systems is
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas b 123 POC system cobas b 123 POC system
The Issue: It has been determined that cobas b 123
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare BR Assay for CA 27.29 250 Test Kits
The Issue: Operating range of the ADVIA Centaur systems is
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare ADVIA Centaur Theophylline 2 (THE02) 250 Test 08838753
The Issue: Operating range of the ADVIA Centaur systems is
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare BNP (8-type Natriuretic Peptide) 500 Test kit 02816634
The Issue: Operating range of the ADVIA Centaur systems is
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 220/240V AC
The Issue: Terumo Cardiovascular System (TCVS) has received reports of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 100/120V AC
The Issue: Terumo Cardiovascular System (TCVS) has received reports of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.