Monoject 20 mL Syringe Luer-Lock Tip Soft Pack

Class I - Dangerous

🏥 Medical Devices Recalled: September 20, 2023 Cardinal Health 200 Surgical Instruments Nationwide

What Should You Do?

Check if you have this product:
Product Code: 1182000777; UDI/DI: 10192253034677 - each, 20192253034674 - box, 50192253034675 - case; Lot Numbers: 221201, 221202, 221203, 221204, 221205, 230201, 230202, 230203, 230204, 230205, 230206
Do not eat it: Even if it looks and smells fine, do not consume this product.
Throw it away or return it: You can return the product to the store for a full refund.
Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
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:: Cardinal Health 200, LLC
Reason for Recall:: Demonstrated recognition and compatibility issues with syringe infusion pumps.
Classification:: Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
Status:: ongoing

Product Information

Full Description:

Monoject 20 mL Syringe Luer-Lock Tip Soft Pack

Product Codes/Lot Numbers:

Product Code: 1182000777; UDI/DI: 10192253034677 - each, 20192253034674 - box, 50192253034675 - case; Lot Numbers: 221201, 221202, 221203, 221204, 221205, 230201, 230202, 230203, 230204, 230205, 230206

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0148-2024

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Class I - Dangerous

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Class I - Dangerous

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