Cardinal Health is recalling Monoject syringes due to manufacturing changes. Affected models include 1, 3, 6, 12, 20, 35, and 60 mL sizes. No specific action is required but check for lot numbers.
Cardinal Health is expanding their previous product correction actions to a product removal of all sizes of Cardinal Health brand Monoject sterile Syringe Luer-Lock (1, 3, 6, 12, 20, 35, and 60 mL) and Cardinal Health brand Monoject sterile Enteral Syringes with the ENFit connection (1, 3, 6, 12, 35, and 60 mL) due to a change in manufacturing and rebranding efforts.
Cardinal Health is recalling all sizes of Monoject syringes and enteral syringes with ENFit connections because of a manufacturing change. This recall does not pose a safety risk but is part of a rebranding effort.
The recall is due to a change in manufacturing and rebranding efforts, not a safety hazard. The product is being removed from the market as part of a company correction action.
People who own or use Cardinal Health Monoject syringes (1, 3, 6, 12, 20, 35, or 60 mL) or enteral syringes with ENFit connections are affected. Those most at risk are users who have the specific lot numbers listed.
Check for the product name 'Cardinal Health Monoject' with sizes 1, 3, 6, 12, 20, 35, or 60 mL. Look for lot numbers 221201, 230201, 230601, or 230602 on the packaging.
Review the product label for the lot numbers 221201, 230201, 230601, or 230602.
No, this recall is part of a manufacturing change and rebranding effort, not a safety hazard.
No action is required; this recall is for product removal due to manufacturing changes, not safety risks.
Lot numbers 221201, 230201, 230601, and 230602 are affected.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0856-2024 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0856-2024 from Cardinal Health. 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.
