FDA Device recall Z-1853-2017
NAMIC Fluid Delivery Set - 72" (183cm) UPN H965913000051, Catalog 91300005
- FDA Device
- Class II
- terminated
- Published 2017-04-26
On 2017-04-26 the FDA classified a Class II recall of NAMIC Fluid Delivery Set - 72" (183cm) UPN H965913000051, Catalog 91300005 by Angiodynamics Navilyst Medical, citing the product has the potential to be non-sterile as it was not packaged in accordance to specification.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1853-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-01-13 |
| Published | 2017-04-26 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Angiodynamics Navilyst Medical |
| Distribution | CA, KY, MD, OR, TX, VA |
Product
NAMIC Fluid Delivery Set - 72" (183cm) UPN H965913000051, Catalog 91300005
Reason
The product has the potential to be non-sterile as it was not packaged in accordance to specification.
Identifiers
| code_info | Lot Number: 5122528 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1853-2017%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.