Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Weck EFx Classic Fascial Closure System Recalled by Teleflex Medical Due to Incorrect expiration date was printed on the product...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Teleflex Medical directly.
Affected Products
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
Quantity: 45
Why Was This Recalled?
Incorrect expiration date was printed on the product label.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teleflex Medical
Teleflex Medical has 204 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report