FDA Device recall Z-1780-2019
Neff Percutaneous Access Set, Catalog Number NPAS-100-RH-NT
- FDA Device
- Class II
- terminated
- Published 2019-06-19
On 2019-06-19 the FDA classified a Class II recall of Neff Percutaneous Access Set, Catalog Number NPAS-100-RH-NT by Cook, citing the products may have been manufactured without the bottom seal on the outer packaging, compromising the sterility of the product.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1780-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-05-02 |
| Published | 2019-06-19 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Cook |
| Distribution | n/a |
Product
Neff Percutaneous Access Set, Catalog Number NPAS-100-RH-NT
Reason
The products may have been manufactured without the bottom seal on the outer packaging, compromising the sterility of the product.
Identifiers
| code_info | lot 8373482 |
|---|
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-1780-2019%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.