ICU Medical recalls specific oncology kits due to potential leakage in certain lots of Sprios male luer fittings. This could lead to fluid leakage during patient administration. Affected kits have lot number 5142959.
Due to molding defect, there is a potential that certain lots of spinning and non-spinning Sprios male luers may exhibit small amounts of leakage in the inactivated position.
ICU Medical is recalling a specific oncology kit that may leak small amounts of fluid when in the inactivated position due to a molding defect. This could cause unintended fluid exposure during patient treatment.
The molding defect in certain lots of Sprios male luer fittings may cause small amounts of fluid leakage when the kit is in the inactivated position. This leakage could potentially lead to unintended fluid exposure during patient administration.
Healthcare professionals using the recalled oncology kit for patient fluid administration. Patients receiving treatment with this kit are at minimal risk due to the small leakage potential.
Check for the lot number 514:2959 on the kit. The product includes a 5-inch (13 cm) add-on set with ChemoLock additive port and vented cap. The kit is used for administering fluids to patients through a vein.
Look for the lot number 5142959 on the kit to determine if it is affected.
The recall involves a potential for small fluid leakage during patient administration, but the risk is low due to the small amount of leakage and the specific defect.
Check for the lot number 5142959 on the kit. The product includes a 5-inch (13 cm) add-on set with ChemoLock additive port and vented cap.
Check the lot number to see if it is affected. If it is, contact ICU Medical for further instructions.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1573-2021 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-1573-2021 from ICU Medical. 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.
