FDASeptember 22, 2017device

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Terminated

Brands named

angiodynamics

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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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. — Recall Details · AllClear