ICU Medical recalls 20mL syringes with spinning Spiros male luer fittings due to a molding defect that may cause small fluid leakage when inactivated. Affected lots include 5109274 and 5125259.
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 20mL syringes with spinning Spiros male luer fittings (red cap) because a molding defect may cause small fluid leakage when the syringe is inactivated. This could lead to improper fluid administration during medical procedures.
A molding defect in the syringe's spinning Spiros male luer fitting can cause small amounts of fluid to leak when the syringe is inactivated. This leakage may occur during medical procedures where precise fluid administration is critical.
Healthcare professionals and patients using the recalled syringes for fluid administration. Those most at risk are individuals administering fluids through these syringes in medical settings.
Look for syringes with a red cap and model REF CH2020. Affected lots are 5109274 and 5125259. These syringes are used for administering fluids into a patient's vascular system.
Verify the lot number on the syringe's packaging to see if it matches 5109274 or 5125259.
The recall is due to a molding defect that may cause small fluid leakage when the syringe is inactivated, potentially affecting medical procedures.
Check the lot number on the syringe's packaging; affected lots are 5109274 and 5125259. These syringes have a red cap and model REF CH2020.
The recall does not specify a remedy, so contact ICU Medical directly for guidance on handling the syringe.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1576-2021 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-1576-2021 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.
