FDA Device recall Z-2218-2016
Smith and Nephew TWINFIX QUICK-T Knot Pusher Suture Cutter
- FDA Device
- Class II
- terminated
- Published 2016-07-27
On 2016-07-27 the FDA classified a Class II recall of Smith and Nephew TWINFIX QUICK-T Knot Pusher Suture Cutter by Smith And Nephew, citing the device could be subject to breaches of its sterile packaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2218-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-06-15 |
| Published | 2016-07-27 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Smith And Nephew |
| Distribution | US |
Product
Smith and Nephew TWINFIX QUICK-T Knot Pusher Suture Cutter; Part Number: 7209417, for arthroscopic use.
Reason
The device could be subject to breaches of its sterile packaging.
Identifiers
| code_info | Batch numbers: 50412843, 50477278, 50527184 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2218-2016%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.