🔍 RecallPedia

Coviden Monoject 60ml Syringe Luer-Lock Tip-used to inject fluid into or withdraw fluids from the body MMS Catalog Number: 1159851 Cardinal Catalog Number: 8881560125

Class I - Dangerous
🏥 Medical Devices Recalled: April 23, 2024 Mckesson Medical-Surgical Inc. Corporate Office Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI-DI: 20884521012230 Lot Code: 330737X
  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:
Mckesson Medical-Surgical Inc. Corporate Office
Reason for Recall:
Quarantined product was inadvertently distributed
Classification:
Class I - Dangerous

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

Status:
completed

Product Information

Full Description:

Coviden Monoject 60ml Syringe Luer-Lock Tip-used to inject fluid into or withdraw fluids from the body MMS Catalog Number: 1159851 Cardinal Catalog Number: 8881560125

Product Codes/Lot Numbers:

UDI-DI: 20884521012230 Lot Code: 330737X

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2039-2024

Related Recalls