🔍 RecallPedia

Sterile Co-Flex NL 4" - Product Usage: Single Use secondary wound dressing or compression wrap

Class I - Dangerous
🏥 Medical Devices Recalled: June 19, 2019 Andover Healthcare Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Manufacturer's product or Catalog # 5400S Expiration Date: 01OCT2021-14JUN2022 Lot # CI0PVV, CI0V78, CI0X0B, CI16CG, CI17BB, CI18KB, CI18Y7, CI1E36, CI1JCE
  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:
Andover Healthcare Inc.
Reason for Recall:
Incomplete packaging seal of sterile product
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Sterile Co-Flex NL 4" - Product Usage: Single Use secondary wound dressing or compression wrap

Product Codes/Lot Numbers:

Manufacturer's product or Catalog # 5400S Expiration Date: 01OCT2021-14JUN2022 Lot # CI0PVV, CI0V78, CI0X0B, CI16CG, CI17BB, CI18KB, CI18Y7, CI1E36, CI1JCE

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0180-2020

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