FDA Device recall Z-2227-2014
Double Offset Rasp Handle, Right Hand A/S Rasp Handle (Right)
- 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, Right Hand A/S Rasp Handle (Right) 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-2227-2014 |
| 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, Right Hand A/S Rasp Handle (Right)
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 00780803522 Lot Number 56474889, 56474890, 56474895, 56474896 |
|---|
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-2227-2014%22
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