Recall Z-0846-2019— Teleflex Medical
Class II · Terminated
Class II FDA medical device recall by Teleflex Medical, initiated 2019-01-07, terminated 2021-11-04. FDA's recall record names no specific 510(k) clearance for this event. Product: Pilling COOLEY SUMP-SUCTION TUBE, REF 351547. Reason: The internal tip is missing from the device, causing the device to not function as intended..
- Recalling firm
- Teleflex Medical
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-01-07
- Terminated
- 2021-11-04
- Firm location
- Research Triangle Park, NC, United States
Product description
Pilling COOLEY SUMP-SUCTION TUBE, REF 351547
Reason for recall
The internal tip is missing from the device, causing the device to not function as intended.
Data sourced from openFDA. This site is unofficial and independent of the FDA.