ICU Medical recalls specific 30" admin sets with a molding defect that may cause leakage in the inactivated position. Affected units include Lot 5142971. Consumers should check product details and contact the company for remedies.
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 model of 30-inch IV administration set due to a molding defect that could cause small leaks when the device is in the inactivated position. This defect might lead to fluid leakage during medical use, potentially affecting patient safety.
The molding defect in the admin set can cause small amounts of fluid to leak when the device is in the inactivated position. This leakage could potentially lead to fluid loss or contamination during medical procedures.
Healthcare professionals using the recalled admin set for patient fluid administration are most at risk. Patients receiving treatment with this specific model may be affected if the leakage occurs.
Check for the product name: 30" (76 cm) Appx 3.2 ml, 20 Drop Admin Set w/Integrated Clave Drip Chamber, Spiros, Bag Hanger. The affected lot number is 5142971.
Identify the product name and lot number to confirm if it matches the recalled items.
The recall states there is a molding defect that may cause small amounts of leakage in the inactivated position.
Check for the product name: 30" (76 cm) Appx 3.2 ml, 20 Drop Admin Set w/Integrated Clave Drip Chamber, Spiros, Bag Hanger and lot number 5142971.
The recall does not specify a remedy, so contact ICU Medical directly 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-1567-2021 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-1567-2021 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.
