PT113950 PT HYBRID Glenoid Post Regenerex porous titanium construct… — Class II medical device recall Z-0660-2013
Terminated recall by Biomet, Inc., reported 2013-01-16, distributed nationwide. Biomet is recalling Part Number PT-113950 PT Hybrid Glenoid Post, following an investigation which identified
| Recall number | Z-0660-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2006-12-12 |
| Classified | 2013-01-09 |
| Reported by FDA | 2013-01-16 |
| Terminated | 2013-11-08 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, AU, CA, CL, JP, NL |
| Quantity | 1,050 |
| Lot numbers | 093540, 093550, 093570, 093580, 093590, 093600, 093610, 093620, 093720, 093730, 093740, 093760, 093770, 093780, 282590, 282600, 282620, 282630, 282680, 282700, 282710, 489160, 489180, 489200, 489210, 489770, 489780, 489790, 714480, 714550, 714570, 714700, 714730, 722210, 722250, 722280, 984770, 984780, 984790, 984800 and 5 more |
| Model numbers | 113950 |
Product
PT113950 PT HYBRID Glenoid Post Regenerex porous titanium construct Sterile R Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
Reason for recall
Biomet is recalling Part Number PT-113950 PT Hybrid Glenoid Post, following an investigation which identified that the male thread of the post may be oversized. This oversized condition can vary in degree and may lead to the following three events: 1) If the PT Hybrid Glenoid Post is not fully seated into the Hybrid Base and the implant construct is implanted, then a gap of 1-3 mm will be prese
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0660-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.