Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Weck Facial Closure Systems have application in laparoscopic procedures for Recalled by Teleflex Medical Due to The devices wings may become partially detached from...
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 Facial Closure Systems have application in laparoscopic procedures for approximation of tissues and percutaneous suturing for closing incision sites.
Quantity: 2265 units
Why Was This Recalled?
The devices wings may become partially detached from the EFx Shield during use.
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