Smith and Nephew TWINFIX QUICK-T Knot Pusher Suture Cutter — Class II medical device recall Z-2218-2016
Terminated recall by Smith & Nephew, Inc., reported 2016-07-27, distributed nationwide. The device could be subject to breaches of its sterile packaging.
| Recall number | Z-2218-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smith & Nephew, Inc., Mansfield, MA, United States |
| Recall initiated | 2016-06-15 |
| Classified | 2016-07-18 |
| Reported by FDA | 2016-07-27 |
| Terminated | 2021-03-22 |
| Distributed | Nationwide (US) |
| Quantity | 563 |
| Reason classes | sterility |
| Lot numbers | 50412843, 50477278, 50527184 |
| Model numbers | 7209417 |
Product
Smith and Nephew TWINFIX QUICK-T Knot Pusher Suture Cutter; Part Number: 7209417, for arthroscopic use.
Reason for recall
The device could be subject to breaches of its sterile packaging.
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-2218-2016. 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.