ICU Medical recalls two types of Spinning Spiros male luers due to a molding defect that may cause small leakage in the inactivated position. This could lead to fluid administration issues during medical procedures.
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 two specific types of Spinning Spiros male luers (red cap and purple cap) because a molding defect might cause small amounts of leakage when the device is in the inactivated position. This leakage could potentially cause fluid administration issues during medical procedures.
A molding defect in the device can cause small amounts of leakage when the luer is in the inactivated position. This leakage could potentially lead to fluid administration issues during medical procedures, such as incorrect dosing or unintended fluid loss.
Healthcare professionals using these specific male luers for administering fluids to patients are most at risk. Patients receiving treatments through these devices may experience fluid administration issues if leakage occurs.
Check for the red cap or purple cap on the Spinning Spiros male luer. The product was sold with lot numbers 5125300 and 5125296.
Look for the red cap or purple cap on the Spinning Spiros male luer to identify if it is part of the recall.
Due to a molding defect, certain lots of spinning and non-spinning Sprios male luers may exhibit small amounts of leakage in the inactivated position.
The leakage could potentially cause fluid administration issues during medical procedures, such as incorrect dosing or unintended fluid loss.
Check for the red cap or purple cap on the Spinning Spiros male luer. The product was sold with lot numbers 5125300 and 5125296.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1586-2021 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-1586-2021 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.
