Neff Percutaneous Access Set — Class II medical device recall Z-1780-2019
Terminated recall by Cook Inc., reported 2019-06-19. The products may have been manufactured without the bottom seal on the outer packaging, compromising the steri
| Recall number | Z-1780-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cook Inc., Bloomington, IN, United States |
| Recall initiated | 2019-05-02 |
| Classified | 2019-06-13 |
| Reported by FDA | 2019-06-19 |
| Terminated | 2019-08-23 |
| Countries outside the US | CN |
| Quantity | 97 |
| Reason classes | sterility, packaging |
| Lot numbers | 8373482 |
| Model numbers | NPAS-100-RH-NT |
Product
Neff Percutaneous Access Set, Catalog Number NPAS-100-RH-NT
Reason for recall
The products may have been manufactured without the bottom seal on the outer packaging, compromising the sterility of the product.
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-1780-2019. 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.