FDA Device recall Z-2186-2012
TAUT, Cholangiogram Catheter Intraducer, Peritoneal Catheter, Teleflex Medical, Research Triangle Park, NC. An introduction/drainage cathet…
- FDA Device
- Class III
- terminated
- Published 2012-08-22
On 2012-08-22 the FDA classified a Class III recall of TAUT, Cholangiogram Catheter Intraducer, Peritoneal Catheter, Teleflex Medical, Research Triangle Park, NC. An introduction/drainage cathet… by Teleflex Medical, citing product is missing the label on the internal packaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2186-2012 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2012-07-20 |
| Published | 2012-08-22 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Teleflex Medical |
| 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 |
Product
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.
Reason
Product is missing the label on the internal packaging.
Identifiers
| code_info | Catalog number: PI-128, Lot number: 01C200424, 01C1200425 and 01C1200426. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2186-2012%22
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