Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
TAUT Recalled by Teleflex Medical Due to Product is missing the label on the internal...
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
TAUT, Cholangiogram Catheter Intraducer, Peritoneal Catheter, Teleflex Medical, Research Triangle Park, NC. An introduction/drainage catheter accessory is intended to aid in the manipulation of or insertion of the device into the body.
Quantity: 611 units
Why Was This Recalled?
Product is missing the label on the internal packaging.
Where Was This Sold?
This product was distributed to 26 states: AL, AK, AZ, CA, CO, FL, GA, IL, IN, IA, KS, LA, MA, MI, MS, MO, NY, NC, OH, PA, SD, 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