Versafitcup Impacting Ring Model Number: 01 — Class II medical device recall Z-0878-2013
Terminated recall by Medacta Usa Inc, reported 2013-03-06, distributed nationwide. Medacta USA is recalling Versafitcup Impacting Ring because the impaction ring may not fit properly in the imp
| Recall number | Z-0878-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medacta Usa Inc, Camarillo, CA, United States |
| Recall initiated | 2010-01-15 |
| Classified | 2013-02-22 |
| Reported by FDA | 2013-03-06 |
| Terminated | 2013-02-23 |
| Distributed | Nationwide (US) |
| Quantity | 293 units |
| Lot numbers | 0133, 0134, 0135, 0136, 0137, 0138, 0139, 0140, 0141, 0142, 095920, 095921, 095922, 095923, 095924, 095925, 095926, 095927, 095928, 095929, 096050, 096050A, 096051, 096051A, 096052, 096052A, 096053, 096053A, 096054, 096054A, 096055, 096055A, 096056, 096056A, 096057, 096057A, 096058, 096058A, 096059, 096059A |
| Model numbers | 0133 |
Product
Versafitcup Impacting Ring Model Number: 01.26.10.0133 (46mm), 01.26.10.0134 (48mm), 01.26.10.0135 (50mm), 01.26.10.0136 (52mm), 01.26.10.0137 (54mm), 01.26.10.0138 (56mm), 01.26.10.0139 (58mm), 01.26.10.0140 (60mm), 01.26.10.0141 (62mm), 01.26.10.0142 (64mm). Designed for cementless use in total hip arthroplasty.
Reason for recall
Medacta USA is recalling Versafitcup Impacting Ring because the impaction ring may not fit properly in the implant shell in all cases. This could result in surgical delay potentially increasing possible complications under anesthesia, having to ream up to a larger shell size leaving less bone than planned and repositiong/removal of the shell after initial impaction.
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-0878-2013. 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.