🔍 RecallPedia

MIC* Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors - 20 Fr-PULL

Class I - Dangerous
🏥 Medical Devices Recalled: December 22, 2021 Avanos Medical Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    1) Code 8160-20, Lot 30135103 2) Code 8640-20, Lot 30132544
  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:
Avanos Medical, Inc.
Reason for Recall:
The External Retention Bolster contained in the kit may be a larger diameter than the tube.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

MIC* Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors - 20 Fr-PULL

Product Codes/Lot Numbers:

1) Code 8160-20, Lot 30135103 2) Code 8640-20, Lot 30132544

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0566-2022

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