Recall Z-2186-2012— Teleflex Medical
Class III · Terminated
Class III FDA medical device recall by Teleflex Medical, initiated 2012-07-20, terminated 2015-02-12. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Teleflex Medical
- Classification
- Class III
- Status
- Terminated
- Initiated
- 2012-07-20
- Terminated
- 2015-02-12
- Firm location
- Research Triangle Park, NC, United States
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.
Reason for recall
Product is missing the label on the internal packaging.
Data sourced from openFDA. This site is unofficial and independent of the FDA.