Recall Z-2218-2016— Smith & Nephew, Inc.
Class II · Terminated
Class II FDA medical device recall by Smith & Nephew, Inc., initiated 2016-06-15, terminated 2021-03-22. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Smith & Nephew, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-06-15
- Terminated
- 2021-03-22
- Firm location
- Mansfield, MA, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.