🔍 RecallPedia

General Plastics Pack, part number 008617-1

Class I - Dangerous
🏥 Medical Devices Recalled: January 11, 2017 Windstone Medical Packaging Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot number and expiration date 85096, 12/11/2017 85458, 12/20/2017 88364, 12/27/2017 89172, 9/3/2018 95260, 9/20/2018 95790, 9/9/2018 96288, 9/18/2018 96562, 9/20/2018 97526, 9/27/2018 97560, 9/13/2018 99232, 2/1/2019 99232, 2/1/2019
  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:
Windstone Medical Packaging, Inc.
Reason for Recall:
The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

General Plastics Pack, part number 008617-1

Product Codes/Lot Numbers:

Lot number and expiration date 85096, 12/11/2017 85458, 12/20/2017 88364, 12/27/2017 89172, 9/3/2018 95260, 9/20/2018 95790, 9/9/2018 96288, 9/18/2018 96562, 9/20/2018 97526, 9/27/2018 97560, 9/13/2018 99232, 2/1/2019 99232, 2/1/2019

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1307-2017

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