🔍 RecallPedia

Resect. Intest. Laparo-LF, Model DYNJ42667A - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.

Class I - Dangerous
🏥 Medical Devices Recalled: November 13, 2020 Medline Industries Diagnostic Equipment

What Should You Do?

  1. Check if you have this product:
    Lot 20GBA365 (Expiration 11/30/2024), 20HBM367 (Expiration 11/30/2024), 20IBC934 (Expiration 11/30/2024)
  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:
Medline Industries Inc
Reason for Recall:
The cylindrical sponge component is not x-ray detectable.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Resect. Intest. Laparo-LF, Model DYNJ42667A - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.

Product Codes/Lot Numbers:

Lot 20GBA365 (Expiration 11/30/2024), 20HBM367 (Expiration 11/30/2024), 20IBC934 (Expiration 11/30/2024)

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0779-2021

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