SYNOVO HIP COMPONENTS 01-03-0047Recalls & reported problems
Synovo Production · HIP FEMORAL RESURFACING CUP - 47 MM · Class 2 · Implant
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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- May 30, 2023Open, Classified
Medical device components were marketed without FDA clearance
Z-1498-2024 · Root cause: No Marketing Application · 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 US157340Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
- Recap Hip System US157344Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
- Recap Hip System US157342Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
- Recap Hip System US157346Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
- SYNOVO HIP COMPONENTS 01-03-0045Synovo Production · Prosthesis, Hip, Femoral, Resurfacing1 recall0 reports
- Recap Hip System US157356Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
- SYNOVO HIP COMPONENTS 01-03-0049Synovo Production · Prosthesis, Hip, Femoral, Resurfacing1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.