FDA Device recall Z-2219-2014
VI DBL OFFST W/ LRG STPL, LT Nonsterile
- FDA Device
- Class II
- terminated
- Published 2014-08-20
On 2014-08-20 the FDA classified a Class II recall of VI DBL OFFST W/ LRG STPL, LT 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-2219-2014 |
| 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
VI DBL OFFST W/ LRG STPL, LT 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 82016757841 Lot Number 97009219, 97009254 |
|---|
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-2219-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.