Product Wiki · Recalls · U.S. FDA — Device Enforcement

TAUT, Cholangiogram Catheter Intraducer, Peritoneal Catheter… — recall Z-2186-2012

U.S. FDA — Device Enforcement · United States · 2012-07-20 · Class III

As described by U.S. FDA — Device Enforcement: 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.

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked on this page. No AI-generated text appears on this page. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2186-2012
Date of alert
2012-07-20
Country / jurisdiction
United States
Risk level
Class III
Notice type
recall
Brand
Teleflex Medical
Product category
device
Product type
Devices
Recall status
Terminated — the recall action is complete and the FDA has closed it
Initiated by
Voluntary: Firm initiated
Distribution
AK, AL, AZ, CA, CO, FL, GA, IA, IL, IN, KS, LA, MA, MI, MO, MS, NC, NY, OH, PA, SD, TX, UT, VA, WI, WV.
Reported risk: Product is missing the label on the internal packaging.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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