FDA Device recall Z-2223-2014
Vl DBL OFFST WI LRG STPL, RT Nonsterile
- FDA Device
- Class II
- terminated
- Published 2014-08-20
On 2014-08-20 the FDA classified a Class II recall of Vl DBL OFFST WI LRG STPL, RT 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-2223-2014 |
| 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
Vl DBL OFFST WI LRG STPL, RT 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 82016757942 Lot Number 97009220, 97009255, 97009256, 97009585 |
|---|
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-2223-2014%22
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