Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE — Class II medical device recall Z-2260-2014
Terminated recall by Angiodynamics, Inc., reported 2014-08-27, distributed nationwide. AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire have the potential to contain an in
| Recall number | Z-2260-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Angiodynamics, Inc., Queensbury, NY, United States |
| Recall initiated | 2014-08-06 |
| Classified | 2014-08-18 |
| Reported by FDA | 2014-08-27 |
| Terminated | 2017-03-27 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, CH, IE, MY, SE |
| Lot numbers | 4731639 |
| Model numbers | 12401806 |
| Expiration dates | 2017-03-31 |
Product
Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE, 5F x 90 cm x 10 cm Infusion Pattern, Catalog No./REF 12401806, Product No. H787124018065, STERILE -- AngioDynamics, 603 Queensbury Avenue, Queensbury, NY 12804
Reason for recall
AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire have the potential to contain an incorrect sized guidewire (too long).
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-2260-2014. 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.