Aesculap Columbus Revision CoCr 15mm distal and posterior spacers — Class II medical device recall Z-0492-2014
Terminated recall by Aesculap, Inc., reported 2013-12-25, distributed in FL, MD. The Columbus Revision CoCr 15 mm distal and posterior implant spacers, sizes F5-F7, were not compatible.
| Recall number | Z-0492-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aesculap, Inc., Center Valley, PA, United States |
| Recall initiated | 2013-09-19 |
| Classified | 2013-12-13 |
| Reported by FDA | 2013-12-25 |
| Terminated | 2014-12-22 |
| Distributed | FL, MD |
| Quantity | 24 |
| Lot numbers | 51447588, 51447597, 51468302, 51468773, 51503760, 51571394, 51585136 |
Product
Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
Reason for recall
The Columbus Revision CoCr 15 mm distal and posterior implant spacers, sizes F5-F7, were not compatible.
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-0492-2014. 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.