🔍 RecallPedia

ANGIO PACK #2; REF: DYNJ39185; Packaged in Mexico by: Medline Industries, Inc., Mundelein, IL 60060; 1-800-Medline; www.medline.com Surgical kit used to supply tools required to perform angiography medical procedures.

Class I - Dangerous
🏥 Medical Devices Recalled: August 14, 2013 Medline Industries Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    Pack Number: DYNJ39185; Lots: 13EB2046, 13FB1553, 13GB2605
  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:
Medline Industries, Inc.
Reason for Recall:
Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the coating to flake off of the wire. The guidewire is used in a number of surgical convenience kits assembled and marketed by Medline Industries, Inc.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

ANGIO PACK #2; REF: DYNJ39185; Packaged in Mexico by: Medline Industries, Inc., Mundelein, IL 60060; 1-800-Medline; www.medline.com Surgical kit used to supply tools required to perform angiography medical procedures.

Product Codes/Lot Numbers:

Pack Number: DYNJ39185; Lots: 13EB2046, 13FB1553, 13GB2605

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1047-2014

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