ConvaTec Active Life, One-Piece Drainable Pouch, 3/4-2 1/2 in., 19-64mm, REF 400599. For the management of stoma output following a colostomy or ileostomy procedure.

Class I - Dangerous
🏥 Medical Devices Recalled: August 16, 2022 ConvaTec Infusion Pumps Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI/DI: 768455102907, Batch numbers: 2A03486, 2B00301
  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:
ConvaTec, Inc
Reason for Recall:
impaired functionality of the release liner
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

ConvaTec Active Life, One-Piece Drainable Pouch, 3/4-2 1/2 in., 19-64mm, REF 400599. For the management of stoma output following a colostomy or ileostomy procedure.

Product Codes/Lot Numbers:

UDI/DI: 768455102907, Batch numbers: 2A03486, 2B00301

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0130-2023

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