NAMIC Fluid Delivery Set — Class II medical device recall Z-1853-2017
Terminated recall by Angiodynamics Inc. (Navilyst Medical Inc.), reported 2017-04-26, distributed in CA, KY, MD, OR, TX, VA. The product has the potential to be non-sterile as it was not packaged in accordance to specification.
| Recall number | Z-1853-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Angiodynamics Inc. (Navilyst Medical Inc.), Glens Falls, NY, United States |
| Recall initiated | 2017-01-13 |
| Classified | 2017-04-18 |
| Reported by FDA | 2017-04-26 |
| Terminated | 2018-06-25 |
| Distributed | CA, KY, MD, OR, TX, VA |
| Reason classes | sterility |
| Lot numbers | 5122528 |
| Model numbers | 91300005 |
Product
NAMIC Fluid Delivery Set - 72" (183cm) UPN H965913000051, Catalog 91300005
Reason for recall
The product has the potential to be non-sterile as it was not packaged in accordance to specification.
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-1853-2017. 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.