FDA Device recall Z-2218-2014
Double Offset Rasp Handle, Left Hand Nonsterile
- FDA Device
- Class II
- terminated
- Published 2014-08-20
On 2014-08-20 the FDA classified a Class II recall of Double Offset Rasp Handle, Left Hand 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-2218-2014 |
| 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
Double Offset Rasp Handle, Left Hand 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 82016757831 Lot Number 97008287, 97900066, 97900084, 97900106, 97900158 |
|---|
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-2218-2014%22
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