Pilling COOLEY SUMP-SUCTION TUBE — Class II medical device recall Z-0846-2019
Terminated recall by Teleflex Medical, reported 2019-02-27, distributed in DC, NY, TX. The internal tip is missing from the device, causing the device to not function as intended.
| Recall number | Z-0846-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Research Triangle Park, NC, United States |
| Recall initiated | 2019-01-07 |
| Classified | 2019-02-16 |
| Reported by FDA | 2019-02-27 |
| Terminated | 2021-11-04 |
| Distributed | DC, NY, TX |
| Countries outside the US | PH |
| Quantity | 80 units |
| Model numbers | 351547 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0846-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.