Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Monofilament and Multifilament Non-absorbable Steel Suture Recalled by Teleflex Medical Due to The products are being recalled because they did...
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
Monofilament and Multifilament Non-absorbable Steel Suture; Product Codes: 0520197-2, 29-727, 29-7270M4, 29-7281M4, E29-5553M4, E29-7270M4, E29-7272M4, E29-727A, EP4013P, EP4110N, X-2235, X29-7271M2, X-5667M8 and X-6730M5.
Quantity: 3,816 ea
Why Was This Recalled?
The products are being recalled because they did not meet minimum diameter requirements.
Where Was This Sold?
This product was distributed to 8 states: CA, CO, FL, IN, KY, MA, NM, PA
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