Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Deknatel Teleflex Medical Stainless Steel 2 (metric 5) Monofilament Stainless Recalled by Teleflex Medical Due to Product does not meet minimum needle attachment strength...
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
Deknatel Teleflex Medical Stainless Steel 2 (metric 5) Monofilament Stainless Steel Suture, Nonabsorbable Surgical Suture, U.S.P. Used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.
Quantity: 32,271 ea.
Why Was This Recalled?
Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use.
Where Was This Sold?
This product was distributed to 28 states: AL, CA, FL, GA, IL, IN, KS, LA, ME, MA, MI, MN, MS, MO, NV, NJ, NM, NY, OH, PA, RI, SC, TN, TX, UT, VA, WV, WI
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