Cardinal Health recalls 60mL Monoject syringes with Luer-Lock tips due to compatibility issues with infusion pumps. Affected units sold in 2019-2023 with specific lot numbers. Stop using immediately to avoid potential recognition errors.
Demonstrated recognition and compatibility issues with syringe infusion pumps.
Cardinal Health is recalling 60mL Monoject syringes with Luer-Lock tips because they may not work properly with some infusion pumps. This could lead to incorrect dosing if the syringe is used with certain pumps. Affected units have specific lot numbers and were sold between 2019 and 2023.
The syringes may not recognize or properly interface with certain infusion pumps, which could cause incorrect dosing or treatment errors. This is a compatibility issue that might not be obvious during normal use but could lead to serious medical consequences if the syringe is used with incompatible pumps.
People who use these syringes with infusion pumps for medical treatments are most at risk. The recall affects patients and healthcare providers who have the specific lot numbers listed.
Check the product code 1186000777T on the syringe packaging. Look for lot numbers 221101 or 230601 on the box or case. These syringes were sold between 2019 and 2023.
Verify the product code 1186000777T and lot numbers 221101 or 230601 on the syringe packaging.
Do not use the syringe with any infusion pump until you confirm it is compatible with your pump model.
The syringes have demonstrated recognition and compatibility issues with certain infusion pumps, which could lead to incorrect dosing.
Lot numbers 221101 and 230601 are affected.
Check the product code 1186000777T and lot numbers 221101 or 230601 on the syringe packaging.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0150-2024 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0150-2024 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.
