Thoracentesis Set — Class II medical device recall Z-1725-2019
Terminated recall by Cook Inc., reported 2019-06-12. Affected products may have been manufactured with the catheter distal end hole too small
| Recall number | Z-1725-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cook Inc., Bloomington, IN, United States |
| Recall initiated | 2019-04-09 |
| Classified | 2019-06-04 |
| Reported by FDA | 2019-06-12 |
| Terminated | 2020-04-28 |
| Countries outside the US | AE, AU, BE, CA, CH, DE, ES, GR, HK, IN, IT, KR, OM, SA |
| Quantity | 5 units |
| Lot numbers | NS7662071 |
Product
Thoracentesis Set, RPN C-THS-850, Order # G03286
Reason for recall
Affected products may have been manufactured with the catheter distal end hole too small
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-1725-2019. 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.