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 35441–35460 of 38,428 recalls
Recalled Item: 00597001303 Femur CR PRC FEM COMP SIZE CML Rx
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597206126 Patella ALL POLY PAT COMP MICRO 26DIA
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597103110 Provisional CR ART SURF PROV 34/STR YEL 10
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00595204110 Articular Surface XLPE CR ART SURF 5-6/STRGRN 10
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00595202010 Articular Surface XLPE CR ART SURF 1
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597003109 Articular Surface CR ART SURF 34/STRIPE YEL 9
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597201101 Femur CR POROUS FEM COMP SIZE AML Rx
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597001333 Femur CR PRC SURF HDN FEM CO-NID CML Rx
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00595501201 Provisional CR-FLEX FEM PROV SZ B-L
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597201333 Femur CR POR SURF HDN FEM CO-NID CML
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597104110 Provisional CR ART SURF PROV 56/STR GRN 10
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597504110 Provisional AC ART SURF PROV 56/STR GRN 10
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00595203110 Articular Surface XLPE CR ART SURF 3
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597203109 Articular Surface CR ART SURF 34/STRIPE YEL 09
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597204109 Articular Surface CR ART SURF 56/STRIPE GRN 9
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597001101 Femur CR PRECOAT FEM COMP SIZE AML
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597101101 Provisional CR PROV FRM COMP SIZE AML
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90595202017 Articular Surface XLPE CR ART SURF AE12/PUR 17
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 65597201101 Femur CR POR FEM HATCP SIZE AML Rx
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597106126 Provisional MIC POROUS PAT PROV 26MMX10MM
The Issue: Surgeons are implanting components of the NexGen Cruciate
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.