Cardinal Health recalls Monoject 0.9% Sodium Chloride Flush Syringes due to potential air reintroduction after expelling air, which could cause inaccurate dosing during IV treatments.
Potential for the plunger to draw back after the air has been expelled and reintroduce air back into the syringe.
Cardinal Health is recalling certain Monoject 0.9% Sodium Chloride Flush Syringes (10 mL) because the plunger might draw back after air expulsion, reintroducing air into the syringe. This could lead to inaccurate medication dosing during intravenous treatments.
The syringe's plunger may retract after air is expelled, causing air to be reintroduced into the syringe. This could result in inaccurate medication dosing when used for intravenous flushes, potentially affecting treatment effectiveness.
Healthcare professionals and patients using intravenous therapy who own the recalled syringes with the listed product codes. Those administering IV treatments are most at risk.
Check for the product code on the syringe label. The recalled syringes have specific product codes listed in the record, including many 19G0814 through 21F1544 codes.
Look for the product code on the syringe label to confirm if it's recalled.
The plunger may draw back after air is expelled, reintroducing air into the syringe, which could cause inaccurate medication dosing during IV treatments.
Check the product code on the syringe label to see if it's in the recalled list. If it is, stop using it and contact Cardinal Health for instructions.
The recall record does not mention a remedy or fix for this issue.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-2284-2021 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-2284-2021 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.
