FDA Device recall Z-0846-2019
Pilling COOLEY SUMP-SUCTION TUBE, REF 351547
- FDA Device
- Class II
- terminated
- Published 2019-02-27
On 2019-02-27 the FDA classified a Class II recall of Pilling COOLEY SUMP-SUCTION TUBE, REF 351547 by Teleflex Medical, citing the internal tip is missing from the device, causing the device to not function as intended.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0846-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-01-07 |
| Published | 2019-02-27 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Teleflex Medical |
| Distribution | DC, NY, TX |
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.
Identifiers
| code_info | Lot/Batch Numbers: A8, C8, I7 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0846-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.