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 34561–34580 of 38,428 recalls
Recalled Item: HERBERT BONE SCREW
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT DEGREE TAPER (various sizes) and FEMORAL HD (various sizes)
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN HUMERAL I/M NAIL. Sizes from 6 MM to 13 MM. Codes starting with 0022541
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERLOCKING IM SCREW SML
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COMPRESSION SCREW (1/2
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12/14 UNIPOLAR FEMORAL HE VERSYS CEM LD/FX SZ 11X12 VERSYS
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRILOGY ACET SHELL 36MM O TRILOGY ACET SHELL 38MM O
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MODULAR AUSTIN MOORE SOLI and MOORE HIP PROS REG SOLID
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEXGEN MIS TIBIA PLATE PR NEXGEN TAPER PLUG NEXGEN PRECOAT
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HGP II ACETABULAR CUP MOD
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HGP II ACETABULAR CUP BON
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6 DEGREE COCR FEM HEAD 36
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERI SCR. 3.5MM X 10MM PERI SCR. 3.5MM X 12MM
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONE-PIECE LAG SCREW 11MM. Item codes starting with 00225900.
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX II KEYLESS TUBE
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I/B II KNEE DOMED PATELLA
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN R-F IM NAIL 9MM DIA
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERLOCKING IM SCREW 4.5 and INTERLOCKING IM SCREW LG Some
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEXGEN OSTEOTOMY CORT BON. Item codes starting with 0052500
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREE-LOCK LAG SCREW
The Issue: Zimmer recently conducted a review of all historic
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.