Teleflex Medical: Medical Device Recall in 2012 - (Recall #: Z-2186-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class III

Date Initiated: July 20, 2012

Date Posted: August 22, 2012

Recall Number: Z-2186-2012

Event ID: 62598

Reason for Recall:

Product is missing the label on the internal packaging.

Status: Terminated

Product Quantity: 611 units

Code Information:

Catalog number: PI-128, Lot number: 01C200424, 01C1200425 and 01C1200426.

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated