Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented
FDA adverse event reports and recall history for hip prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented (product code OQG), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 671
- Deaths
- 0
- Injuries
- 484
- Malfunctions
- 183
Reports per year
Source: FDA adverse event reports by year received, 2004–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
- 2023-08-16Open, ClassifiedError in labeling
CONFORMIS HIP-SCREW-6.5MM X 25MM, STERILE EO
30mm screws were labeled as 25mm screws.
- 2013-04-07TerminatedDevice Design
Stelkast Cross-over Acetabular Shell and Liner Hip System, Part Numbers SC3458-52, SC3474-52, SC3459-52, and SC3460-52. Intended for use in reconstruction of the articulating surface of the acetabular portion of the hip.
Firm was made aware of incidents relating to the difficulty of properly engaging and securing the Cross-Over 36mm liner into the Cross-Over shell.
Monitor hip prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.