# FDA recall Z-0742-2018

> **Angiodynamics, Inc.** · Class II · device recall initiated 2017-09-22.

## 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.

## Distribution

US Distribution to the states of : AL, CA, CT, FL, GA, IL, IN, MD, MI, MN, MO, OH, OR, TX.

## Key facts

- **Recall number:** Z-0742-2018
- **Recalling firm:** Angiodynamics, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-09-22
- **Report date:** 2018-03-07
- **Termination date:** 2018-09-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Queensbury, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0742-2018

## Citation

> AI Analytics. FDA recall Z-0742-2018. Retrieved 2026-07-04 from https://api.ai-analytics.org/recall/Z-0742-2018. Source: US FDA. Licensed CC0.

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