AngioDynamics Angiographic catheter --- Soft-Vu — Class II medical device recall Z-2180-2012
Terminated recall by Angiodynamics Worldwide Headquarters, reported 2012-08-15, distributed nationwide. AngioDynamics is recalling one lot of Soft-Vu Angiographic catheters because one of the catheter pouches withi
| Recall number | Z-2180-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Angiodynamics Worldwide Headquarters, Latham, NY, United States |
| Recall initiated | 2012-06-15 |
| Classified | 2012-08-09 |
| Reported by FDA | 2012-08-15 |
| Terminated | 2016-02-10 |
| Distributed | Nationwide (US) |
| Countries outside the US | CH, CZ |
| Reason classes | labeling |
| Lot numbers | 564325 |
| Model numbers | 10734201 |
Product
AngioDynamics Angiographic catheter --- Soft-Vu (JB-1) Non-braided. --- Size: 5F; Length: 100cm; designed to accept guidewire: .035 in. --- Catalog No. [REF]: 10734201. Packaged in boxes of 5 catheters each, with manufacturer listed as AngioDynamics, Inc., Queensbury, NY USA. Intended use: angiographic diagnosis.
Reason for recall
AngioDynamics is recalling one lot of Soft-Vu Angiographic catheters because one of the catheter pouches within the outer box may be mislabeled.
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-2180-2012. 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.