Angiodynamics, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0742-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: September 22, 2017

Date Posted: March 7, 2018

Recall Number: Z-0742-2018

Event ID: 79193

Reason for Recall:

Product was placed into distribution prior to completion of all required post sterilization release activities.

Status: Terminated

Product Quantity: 28

Code Information:

Lot Number: 5229642; Manufactured 6-Sep-17; Expiration Date: 31-Aug-20

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated