Angiodynamics, Inc. recalls Soft-Vu Omni Flush Angiographic Catheter (UPN H787107322015)
See all recalls from Angiodynamics, Inc. →Recalled 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.
Hazard / Issue
Product was placed into distribution prior to completion of all required post sterilization release activities.
Issued by
FDA
Affected States: AL, CA, CT, FL, GA, IL, IN, MD, MI, MN, MO, OH, OR, TX
Lot/Code Info: Lot Number: 5229642; Manufactured 6-Sep-17; Expiration Date: 31-Aug-20
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Soft-Vu Omni Flush Angiographic →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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