Multipolar¿ Bipolar Cup METAL SHELL 38 MM OD through 71 MM OD — Class II medical device recall Z-0068-2014
Terminated recall by Zimmer, Inc., reported 2013-11-06, distributed nationwide. The low density polyethylene (LDPE) bag used to package implants adheres to the highly polished surface of the
| Recall number | Z-0068-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2013-08-30 |
| Classified | 2013-10-25 |
| Reported by FDA | 2013-11-06 |
| Terminated | 2014-09-25 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, AU, BO, BR, CA, CL, CN, CO, CR, DE, DO, EC, GT, HK, HN, IL, IN, JM, JP, KR, MX, MY, NI, NZ, PA, PE, SG, SV, TH, TW |
| Quantity | 72,806 |
Product
Multipolar¿ Bipolar Cup METAL SHELL 38 MM OD through 71 MM OD. Indicated in fracture dislocation of the hip.
Reason for recall
The low density polyethylene (LDPE) bag used to package implants adheres to the highly polished surface of the devices.
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-0068-2014. 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.