FDA Device recall Z-2230-2014
23.5 Deg Rasp Handle Assy- LEFT Nonsterile
- FDA Device
- Class II
- terminated
- Published 2014-08-20
On 2014-08-20 the FDA classified a Class II recall of 23.5 Deg Rasp Handle Assy- LEFT Nonsterile by Zimmer, citing the firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2230-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-07-23 |
| Published | 2014-08-20 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Zimmer |
| Distribution | US |
Product
23.5 Deg Rasp Handle Assy- LEFT Nonsterile
Reason
The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.
Identifiers
| code_info | Item Number 82-0167-636-00 Lot Number 97009530, 97009782 |
|---|
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-2230-2014%22
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