SYNOVO HIP COMPONENTS 01-03-0051Recalls & reported problems
Synovo Production · HIP FEMORAL RESURFACING CUP - 51MM · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
3 other recalls cover devices cleared under the same FDA submission (K904870); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- May 30, 2023Class IIOpen, Classified
Medical device components were marketed without FDA clearance
Z-1498-2024 · Root cause: No Marketing Application · Recall details · FDA record ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K904870. One submission often covers many models, so check the product and lot details in each record.
- Z-1624-2010 · Jun 5, 2009 · TerminatedEndotec Prothesis Ankle, Titanium Alloy, Sterilized. BP Ankle System, Talar Ankle Component: Size 2 Talar Component Catalog: 05-01-0002, Size 3 Talar Component Catalog: 05-01-000
- Z-1625-2010 · Jun 5, 2009 · TerminatedEndotec Prothesis Ankle, Titanium Alloy, Sterilized, BP Ankle System. BP Ankle System, F-P Type III Ankle Bearing Component: 2x5mm F-P Type III Ankle Bearing Catalog: 05-13-0532,
- Z-1627-2010 · Jun 5, 2009 · TerminatedEndotec Prothesis Ankle, Titanium Alloy, Sterilized, BP Ankle System. BP Ankle System, B-P Type II Talar Ankle Component: Size 1 B-P Type II Talar Ankle Component Catalog: 05-01-
Other Prosthesis, Hip, Femoral, Resurfacing devices
- SYNOVO HIP COMPONENTS 01-03-0044Synovo Production · Prosthesis, Hip, Femoral, Resurfacing1 recall0 reports
- Recap Hip System US157354Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
- Recap Hip System US157356Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
- Recap Hip System US157344Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
- Recap Hip System US157348Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
- Recap Hip System US157352Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
- SYNOVO HIP COMPONENTS 01-03-0045Synovo Production · Prosthesis, Hip, Femoral, Resurfacing1 recall0 reports
- Recap Hip System US157358Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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