ICU Medical recalls certain IV adapters due to potential leakage when inactivated. Affected units may leak small amounts of fluid during use, requiring immediate action to prevent complications.
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 specific IV adapters that could leak small amounts of fluid when in the inactivated position. This leakage risk could lead to complications during medical fluid administration.
The adapters have a molding defect that causes small amounts of fluid to leak when in the inactivated position. This leakage could potentially lead to complications during medical fluid administration if the adapter is not properly secured.
Healthcare professionals using the recalled IV adapters for patient fluid administration are most at risk. Patients receiving treatment through these adapters may be affected if the leakage occurs.
Check for the model REF 034-H2629 with lot number 5125301. The product is used for administering fluids to patients through IV systems.
Inspect the adapter for signs of leakage when in the inactivated position.
This recall applies to specific IV adapters with model REF 034-H2629 and lot number 5125301. Check your equipment to see if it matches these details.
Look for the model REF 034-H2629 and lot number 5125301 on the adapter. The product is used for administering fluids to patients through IV systems.
The recall does not specify a remedy, so contact ICU Medical directly for guidance on next steps.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1584-2021 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-1584-2021 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.
