FDA recall Z-0846-2019
Teleflex Medical · Class II · device
Product
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.
Distribution
TX, NY, DC and Philippines
Key facts
- Status
- Terminated
- Initiation date
- 2019-01-07
- Report date
- 2019-02-27
- Termination date
- 2021-11-04
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Research Triangle Park, NC, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0846-2019