Extremity Components: PROTHESE A EXPANSION COMPLETE D=6 LG 12 MM — Class II medical device recall Z-0185-2013
Terminated recall by Wright Medical Technology Inc, reported 2012-11-07, distributed nationwide. There may be inaccuracies on the labeled shelf life on all products packaged at the Toulon, France facility.
| Recall number | Z-0185-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wright Medical Technology Inc, Arlington, TN, United States |
| Recall initiated | 2012-09-05 |
| Classified | 2012-10-31 |
| Reported by FDA | 2012-11-07 |
| Terminated | 2014-01-07 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BE, BG, BR, CA, CL, CN, CY, CZ, DE, DK, ES, FI, FR, GB, GR, IT, JP, LT, LV, NL, NO, PL, PT, RS, RU, SI, SK, TR, TW, ZA |
| Quantity | 840 units |
| Reason classes | labeling |
| Lot numbers | U11113596, W12372884, W12376849, W12383045, W12383485, X01359005, X01383482, X06391313, X06391315, X06391316, X06396622, X07401148, X07401150, X07401445, X07401448, X07420387, X09401447, X09418985, X09418986, X09418988 |
| Model numbers | PPO90000, PPO90100, PPO90200, PPO90300, PPP70088 |
Product
Extremity Components: PROTHESE A EXPANSION COMPLETE D=6 LG 12 MM, Part Number PPO90000, Lot Numbers: U11113596, W12372884, W12376849, X01383482, X06391313, X07401148, X07401445, and X09418985 PROTHESE A EXPANSION COMPLETE D=8 LG 15 MM, Part Number PPO90100, Lot Number X09418986 PROTHESE A EXPANSION COMPLETE D=10 LG 18 MM, Part Number PPO90200, Lot Numbers: X06391315, X07401150, X07420387, and X09401447 PROTHESE A EXPANSION COMPLETE D=12 LG 20 MM, Part Number PPO90300, Lot Numbers: W12383045, W12383485, X06391316, X06396622, X07401448, and X09418988 TIGE HUMERALE PROXIMALE "NGR" LONG, Part Number PPP70088, Lot Number X01359005 Orthopaedic
Reason for recall
There may be inaccuracies on the labeled shelf life on all products packaged at the Toulon, France facility.
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-0185-2013. 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.