Recall Z-2538-2016— Teleflex Medical
Class II · Terminated
Class II FDA medical device recall by Teleflex Medical, initiated 2016-03-24, terminated 2020-09-25. FDA's recall record names no specific 510(k) clearance for this event. Product: Weck EFx Classic Fascial Closure System, Rx Only, Sterile, The product is intended to facilitate placement and withdrawal of suture loops to repair port side defects following laparoscopic surgery. Reason: Incorrect expiration date was printed on the product label..
- Recalling firm
- Teleflex Medical
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-03-24
- Terminated
- 2020-09-25
- Firm location
- Research Triangle Park, NC, United States
Product description
Weck EFx Classic Fascial Closure System, Rx Only, Sterile, The product is intended to facilitate placement and withdrawal of suture loops to repair port side defects following laparoscopic surgery
Reason for recall
Incorrect expiration date was printed on the product label.
Data sourced from openFDA. This site is unofficial and independent of the FDA.