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
Reported: August 24, 2016 Initiated: March 24, 2016 #Z-2538-2016
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.
Details
- Recalling Firm
- Teleflex Medical
- Units Affected
- 45
- Distribution
- Nationwide Distribution to CA, CO, IA, KS, MD, MI, NY, NC, PA
- Location
- Research Triangle Park, NC
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Teleflex Medical. Units affected: 45.
Why was this product recalled? ▼
Incorrect expiration date was printed on the product label.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 24, 2016. Severity: Moderate. Recall number: Z-2538-2016.
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