Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Dekna-lok Recalled by Teleflex Medical Due to The product did not meet minimum and/or average...
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
Dekna-lok, 1 x 17.78 cm, Violet Braided Polyglycolic Acid Coated Suture, Synthetic Absorbable Surgical Suture USP, Rx Only, Sterile. Teleflex Product Code: 200101-01.
Quantity: 7,380 ea (total)
Why Was This Recalled?
The product did not meet minimum and/or average minimum Teleflex resorption strength requirements.
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