Mckesson Medical-Surgical recalls Coviden Monoject 60ml syringes due to inadvertent distribution of quarantined product. Affected units have specific catalog numbers and lot codes.
Quarantined product was inadvertently distributed
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.
The syringes were distributed without proper quarantine, meaning they could have been contaminated or not meet safety standards. This poses a risk of using unsafe medical devices which could lead to infections or other complications.
Healthcare providers and patients who own or use Coviden Monoject 60ml syringes with Luer-Lock tips. Those with the specific catalog numbers and lot codes listed are most at risk.
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.
Verify the syringe has the MMS Catalog Number 1159851 or Cardinal Catalog Number 8881560125 and Lot Code 330737X.
The syringes were inadvertently distributed as quarantined product, meaning they may not be safe for use.
Check for the MMS Catalog Number 1159851 or Cardinal Catalog Number 8881560125 and Lot Code 330737X on the syringe packaging.
The recall record does not specify a remedy, so contact Mckesson Medical-Surgical for guidance.
We’ve drafted a message you can send Mckesson Medical-Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-2039-2024 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall Z-2039-2024 from Mckesson Medical-Surgical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
