DePuy Synthes PINNACLE Hip System
DePuy Synthes · Hip implants
No recall records foundLast checked Aug 17, 2026
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Reviewed V1 category
Implantable components and systems used in hip replacement procedures.
FDA product codes and descriptions are normalized into this consumer-facing category. Raw regulator terminology remains source evidence rather than separate public category pages.
3 tracked devices · 2 recall records
DePuy Synthes · Hip implants
No recall records foundLast checked Aug 17, 2026
Stryker Corporation · Hip implants
No recall records foundLast checked Aug 17, 2026
Zimmer Biomet · Hip implants
No recall records foundLast checked Aug 17, 2026
Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.
Zimmer Biomet is conducting a medical device recall for two (2) lots of the Dual Mobility Vivacit-E Bearing due to a commingle. The outer package is labeled as a Size F 44 mm, however, the implant inside the package is a Size G 46 mm, and vice versa.
Manufacturers are listed because their devices appear in monitored sources. Listing does not imply endorsement or partnership.
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