FDA Device recall Z-0492-2014
Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
- FDA Device
- Class II
- terminated
- Published 2013-12-25
On 2013-12-25 the FDA classified a Class II recall of Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7 by Aesculap, citing the Columbus Revision CoCr 15 mm distal and posterior implant spacers, sizes F5-F7, were not compatible.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0492-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-09-19 |
| Published | 2013-12-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Aesculap |
| Distribution | FL, MD |
Product
Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7
Reason
The Columbus Revision CoCr 15 mm distal and posterior implant spacers, sizes F5-F7, were not compatible.
Identifiers
| code_info | lots: 51468773, 51447588, 51468302, 51503760, 51571394, 51585136, 51447597 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0492-2014%22
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