🔍 RecallPedia

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.

Class I - Dangerous
🏥 Medical Devices Recalled: September 22, 2017 Angiodynamics Surgical Instruments

What Should You Do?

  1. Check if you have this product:
    Lot Number: 5229642; Manufactured 6-Sep-17; Expiration Date: 31-Aug-20
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Angiodynamics, Inc.
Reason for Recall:
Product was placed into distribution prior to completion of all required post sterilization release activities.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full 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 Codes/Lot Numbers:

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

Distribution:

Distributed in: US, AL, CA, CT, FL, GA, IL, IN, MD, MI, MN, MO, OH, OR, TX

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0742-2018

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