Suture Set, Sterile Single Use, Stage Two: Clean Ready to Use, Latex Free, 20/case, Medical Action Industries, Inc, Arden, NC.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Model number: 58468B, Lot number: 187203, Exp. Date: 11/1/2016.
  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:
Medical Action Industries Inc
Reason for Recall:
Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Suture Set, Sterile Single Use, Stage Two: Clean Ready to Use, Latex Free, 20/case, Medical Action Industries, Inc, Arden, NC.

Product Codes/Lot Numbers:

Model number: 58468B, Lot number: 187203, Exp. Date: 11/1/2016.

Distribution:

Distributed in: AR, AZ, FL, GA, IA, IL, KY, MA, MN, NC, NY, OH, TN, TX, VA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1952-2014

Related Recalls

Potential lack of sterility assurance

Mar 1, 2019 Other Medical Devices Nationwide View Details β†’

Potential compromise of product sterility due to breach of sterile barrier.

Nov 27, 2018 Surgical Instruments View Details β†’

Product sterility potentially compromised.

Dec 11, 2017 Other Medical Devices View Details β†’