🔍 RecallPedia

Halyard, Drape Pack. Kit Code: LMDP36-01.

Class I - Dangerous
🏥 Medical Devices Recalled: April 30, 2026 AVID Medical Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Kit Code: LMDP36-01.UDI-DI: 10809160479148. Lot Number: LMDP36-01. Expiration Date: 9/10/2028
  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:
AVID Medical, Inc.
Reason for Recall:
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Halyard, Drape Pack. Kit Code: LMDP36-01.

Product Codes/Lot Numbers:

Kit Code: LMDP36-01.UDI-DI: 10809160479148. Lot Number: LMDP36-01. Expiration Date: 9/10/2028

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2409-2026

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