Soft-Vu Omni Flush Angiographic Catheter — Class II medical device recall Z-0742-2018
Terminated recall by Angiodynamics, Inc., reported 2018-03-07, distributed in AL, CA, CT, FL, GA, IL, IN, MD…. Product was placed into distribution prior to completion of all required post sterilization release activities
| Recall number | Z-0742-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Angiodynamics, Inc., Queensbury, NY, United States |
| Recall initiated | 2017-09-22 |
| Classified | 2018-02-27 |
| Reported by FDA | 2018-03-07 |
| Terminated | 2018-09-19 |
| Distributed | AL, CA, CT, FL, GA, IL, IN, MD, MI, MN, MO, OH, OR, TX |
| Quantity | 28 |
| Lot numbers | 5229642 |
| Model numbers | 10732201 |
| Expiration dates | 2020-08-31 |
Product
Soft-Vu Omni Flush Angiographic Catheter (UPN H787107322015); SV OF 5F x 65 cm .035 NB PG; Catalog Number: 10732201 AngioDynamics Angiographic Catheters are for use where angiographic diagnosis is indicated.
Reason for recall
Product was placed into distribution prior to completion of all required post sterilization release activities.
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-0742-2018. 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.