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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

Mckesson Medical-Surgical Inc. Corporate Office: Coviden Monoject 60ml Syringes Recalled for Distribution of Quarantined Product

Agency Publication Date: June 7, 2024
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Summary

McKesson Medical-Surgical has recalled 5 boxes (100 units total) of Coviden Monoject 60ml Syringes with Luer-Lock Tips. These medical devices, used to inject or withdraw fluids from the body, were distributed to customers even though they had been placed in quarantine. Because the product was meant to be held and not sold, it may not meet safety or quality standards, and consumers should contact their healthcare provider or the manufacturer for guidance.

Risk

The use of product that was marked for quarantine and inadvertently distributed may pose a risk of infection or device failure if the product was quarantined due to potential contamination or manufacturing defects. No specific injuries or incidents were reported in the recall notice.

What You Should Do

  1. Check your medical supplies for Coviden Monoject 60ml Syringe Luer-Lock Tips with MMS Catalog Number 1159851 or Cardinal Catalog Number 8881560125.
  2. Verify if your product matches UDI-DI 20884521012230 and Lot Code 330737X.
  3. Immediately stop using any syringes identified as part of this recalled lot.
  4. Contact your healthcare provider if you have used these syringes and have concerns about your health or safety.
  5. Contact McKesson Medical-Surgical at their corporate office or your dedicated representative to arrange for the return of the product and to discuss potential refunds.
  6. For additional information, contact the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Contact healthcare provider or manufacturer

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: Coviden Monoject 60ml Syringe Luer-Lock Tip
Model / REF:
1159851
8881560125
Lot Numbers:
330737X

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94595
Status: Resolved
Manufacturer: Mckesson Medical-Surgical Inc. Corporate Office
Sold By: McKesson Medical-Surgical Inc.
Manufactured In: United States
Units Affected: 5 Boxes (20 per box, 100 eaches)
Distributed To: New Jersey

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.