SL PLUS MIA DOUBLE OFFSET ADAPTER RIGHT 60/25MM — Class II medical device recall Z-0730-2019
Terminated recall by Smith & Nephew, Inc., reported 2019-01-23, distributed in NY, TN. The pin that holds the spring mechanism is not properly mounted. The pin could potentially disassemble.
| Recall number | Z-0730-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smith & Nephew, Inc., Memphis, TN, United States |
| Recall initiated | 2019-01-07 |
| Classified | 2019-01-11 |
| Reported by FDA | 2019-01-23 |
| Terminated | 2020-09-17 |
| Distributed | NY, TN |
| Countries outside the US | DE, GB, IT, SG |
| Quantity | 72 units |
| Lot numbers | C63165, C63306, C63495 |
Product
SL PLUS MIA DOUBLE OFFSET ADAPTER RIGHT 60/25MM, S&N 75004613
Reason for recall
The pin that holds the spring mechanism is not properly mounted. The pin could potentially disassemble.
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-0730-2019. 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.