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Angiodynamics, Inc. recalls Soft-Vu Omni Flush Angiographic Catheter (UPN H787107322015); SV OF 5F x 65 cm .035 NB PG; Catalog Number: 10732201 A
Recalled March 7, 2018 · FDA recall Z-0742-2018 · Angiodynamics
Hazard
Product was placed into distribution prior to completion of all required post sterilization release activities. · FDA Class II
Units
28
Sold at
US Distribution to the states of : AL, CA, CT, FL, GA, IL, IN, MD, MI, MN, MO, OH, OR, TX.
Description
Product was placed into distribution prior to completion of all required post sterilization release activities.
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.
Manufacturer(s)
Angiodynamics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →