SMR allen wrench 5 mm — Class II medical device recall Z-2707-2016
Terminated recall by Limacorporate S.p.A, reported 2016-09-07. Product found to be dimensionally non-conforming (slightly over dimensioned on the diameter of the Zimmer conn
| Recall number | Z-2707-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Limacorporate S.p.A, San Daniele Del Friuli, N/A, Italy |
| Recall initiated | 2016-07-21 |
| Classified | 2016-08-31 |
| Reported by FDA | 2016-09-07 |
| Terminated | 2017-01-13 |
| Countries outside the US | AU, IT |
| Quantity | 76 |
Product
SMR allen wrench 5 mm, product code 9013.50.210
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2707-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.