FDA Device recall Z-0730-2019
SL PLUS MIA DOUBLE OFFSET ADAPTER RIGHT 60/25MM, S&N 75004613
- FDA Device
- Class II
- terminated
- Published 2019-01-23
On 2019-01-23 the FDA classified a Class II recall of SL PLUS MIA DOUBLE OFFSET ADAPTER RIGHT 60/25MM, S&N 75004613 by Smith And Nephew, citing the pin that holds the spring mechanism is not properly mounted. The pin could potentially disassemble.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0730-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-01-07 |
| Published | 2019-01-23 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Smith And Nephew |
| Distribution | NY, TN |
Product
SL PLUS MIA DOUBLE OFFSET ADAPTER RIGHT 60/25MM, S&N 75004613
Reason
The pin that holds the spring mechanism is not properly mounted. The pin could potentially disassemble.
Identifiers
| code_info | Lot Numbers: C63165, C63306, C63495 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0730-2019%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.