Cardinal Health recalls 35mL Monoject syringes with Luer-Lock tips due to compatibility problems with infusion pumps. Affected units include specific lot numbers and packaging codes from 2019-2023.
Demonstrated recognition and compatibility issues with syringe infusion pumps.
Cardinal Health is recalling 35mL Monoject syringes with Luer-Lock tips because they may not work properly with certain infusion pumps. This could lead to incorrect dosing or treatment errors if used with incompatible pumps.
These syringes may not recognize or communicate correctly with infusion pumps, leading to incorrect dosing or treatment errors. This could cause unsafe medication delivery if the syringe is used with incompatible pumps.
People using these syringes for medical injections, especially those with infusion pumps, are most at risk. The recall affects specific lot numbers and packaging codes sold between 2019 and 2:06, 2023.
Check for the product code 1183500777 on the syringe, or lot numbers 221201, 230201, 230601, 230602 on the packaging. The syringes come in soft packs with UDI/DI codes starting with 10192253034691.
Look for the product code 1183500777 or lot numbers 221201, 230201, 230601, 230602 on the syringe packaging.
The syringes have demonstrated recognition and compatibility issues with syringe infusion pumps, which could lead to incorrect dosing or treatment errors.
Check for the product code 1183500777 on the syringe or lot numbers 221201, 230201, 230601, 230602 on the packaging.
The recall does not require immediate stoppage; however, users should check compatibility with their infusion pumps before use.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0149-2024 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0149-2024 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.
