FDA Device recall Z-2707-2016
SMR allen wrench 5 mm, product code 9013.50.210
- FDA Device
- Class II
- terminated
- Published 2016-09-07
On 2016-09-07 the FDA classified a Class II recall of SMR allen wrench 5 mm, product code 9013.50.210 by Limacorporate S P A, citing product found to be dimensionally non-conforming (slightly over dimensioned on the diameter of the Zimmer connection) and non-functional for connecting with some T-handles.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2707-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-07-21 |
| Published | 2016-09-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Limacorporate S P A |
| Distribution | n/a |
Product
SMR allen wrench 5 mm, product code 9013.50.210
Reason
Product found to be dimensionally non-conforming (slightly over dimensioned on the diameter of the Zimmer connection) and non-functional for connecting with some T-handles.
Identifiers
| code_info | 14AA311 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Other recalls by Limacorporate S P A
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All Limacorporate S P A recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2707-2016%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.