Unrated Medical device recall · FDA · Published April 23, 2024

Coviden Monoject 60ml Syringe Recall: Quarentined Product Distribution Risk

Mckesson Medical-Surgical recalls Coviden Monoject 60ml syringes due to inadvertent distribution of quarantined product. Affected units have specific catalog numbers and lot codes.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2039-2024Medical device Mckesson Medical-Surgical ›

Recall notice

Quarantined product was inadvertently distributed

Take action

Contact the company

Recalling firmMckesson Medical-Surgical Inc. Corporate Office9954 Maryland Drive, Deep Run Iii Ste. 4000 · Richmond, VA 23233

✎ GovInfoNow plain-language explainer

Mck: Mckesson Medical-Surgical has recalled Coviden Monoject 60ml syringes with Luer-Lock tips because they were inadvertently distributed as quarantined product. This means the syringes may not be safe for use and should be checked against the listed catalog numbers and lot codes. Read more at govinfonow.com/recall/55313-coviden-monoject-60ml-syringe-recall-quarentined-product-distribution-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/55313-coviden-monoject-60ml-syringe-recall-quarentined-product-distribution-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2039-2024

Cite this page

“Coviden Monoject 60ml Syringe Recall: Quarentined Product Distribution Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/55313-coviden-monoject-60ml-syringe-recall-quarentined-product-distribution-risk. Based on FDA recall #Z-2039-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2039-2024%22&limit=1).

The FDA announced on April 23, 2024, that Mckesson Medical-Surgical Inc. Corporate Office is recalling Coviden Monoject 60ml Syringes because quarantined product was inadvertently distributed. The agency issued recall number Z-2039-2024 for the Class II voluntary recall.

How to tell if you have it

Brand: Mckesson Medical-Surgical
Product: Coviden Monoject 60ml Syringe Luer-Lock Tip
MMS Catalog Number: 1159851
Cardinal Catalog Number: 8881560125
UDI-DI: 20884521012230
Lot Code: 330737X

The hazard

The FDA stated that quarantined product was inadvertently distributed. The recall involves Coviden Monoject 60ml Syringes with Luer-Lock Tips used to inject or withdraw fluids.

Context

GovInfoNow's records show Mckesson Medical-Surgical Inc. Corporate Office has 14 other recalls on record since June 2, 2021. Other recent recalls of similar products include Medline Syringes Recall (Feb. 25, 2026) and Medline Convenience Kits with Unapproved Syringes Recalled (Feb. 27, 2026).

How to tell if you have this one

Check for the MMS Catalog Number 1159851 or Cardinal Catalog Number 8881560125 on the syringe. Also look for the Lot Code 330737X on the packaging.

Brand
Mckesson Medical-Surgical
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Verify the syringe has the MMS Catalog Number 1159851 or Cardinal Catalog Number 8881560125 and Lot Code 330737X.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “US Nationwide distribution in the state of NJ.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 57 days after the firm started it.

Apr 23, 2024Firm started the recall
Jun 7, 2024FDA classified it Class II
Jun 19, 2024Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Keep exploring

More Mckesson Medical-Surgical recalls

Link to this recall

<a href="https://govinfonow.com/recall/55313-coviden-monoject-60ml-syringe-recall-quarentined-product-distribution-risk">Coviden Monoject 60ml Syringe Recall: Quarentined Product Distribution Risk (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-2039-2024 (April 23, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2039-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.