Moore Hip Prosthesis Long Fenestrated Stem 38 mm — Class II medical device recall Z-2215-2014
Terminated recall by Zimmer, Inc., reported 2014-08-20, distributed nationwide. Zimmer is initiating a voluntary recall of 20 production lots of Moore Hip Prosthesis Long Fenestrated Stems d
| Recall number | Z-2215-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2014-07-01 |
| Classified | 2014-08-13 |
| Reported by FDA | 2014-08-20 |
| Terminated | 2015-01-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 68 |
| Lot numbers | 62352570, 62396506, 62400669, 62400670, 62424468, 62424469, 62424470, 62435851, 62435852, 62435853, 62435854, 62467218, 62467222, 62470576, 62511377, 62511379, 62511381, 62524114, 62524115 |
| Model numbers | 00402100838, 00402100841, 00402100843, 00402100844, 00402100848, 00402100851, 00402100852, 00402100854, 00402101241, 00402101244, 00402101246, 00402101248, 00402101249, 00402101251, 00402101252, 00402101254, 00402101257, 00402101260, 37108214 |
Product
Moore Hip Prosthesis Long Fenestrated Stem 38 mm (1-1/2 Inch) Head Diameter 203 mm Length. Product Usage: The Moore Hip Prosthesis is a femoral him stem that can be used where there is roentgenogrpahic evidence of a satisfactory actabulum and sufficient bone in the femoral neck to seat the prosthesis with or without bone cement.
Reason for recall
Zimmer is initiating a voluntary recall of 20 production lots of Moore Hip Prosthesis Long Fenestrated Stems due to packaging design verification test failures. Specifically, 9 of 16 test samples failed simulated distribution and shipping testing when the Moore hip stem breached either the inner or outer package tray. Zimmer has not received any complaints of damaged package trays for these 20 lot
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-2215-2014. 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.