ICU Medical recalls a specific intravascular administration set due to a visible gap between connector housings that could lead to disconnections during use.
Due to a manufacturing defect which results in a visible gap between the connector's top and bottom housing.
ICU Medical is recalling a specific intravascular administration set that has a visible gap between the connector's top and bottom housing. This defect could cause the set to disconnect during use, potentially leading to medical complications.
The visible gap in the connector housing can cause the set to disconnect during use. This disconnection could lead to medical complications such as interrupted treatment or fluid leakage.
Healthcare professionals using this specific intravascular set for medical administration are most at risk. Patients receiving treatment with this set could be affected if it disconnects.
Check for the product name: 6.5 IN (17 cm) APPX 0.78 ml, EXT SET w/Clave CLEAR, Clave 4-WAY Stopcock, Spiros, RED CAP. The lot number 5782919 is associated with this recall.
Inspect the connector for a visible gap between the top and bottom housing.
The recall states there is a visible gap that could cause disconnection during use, but the product is not immediately dangerous if the gap is not present.
The recall does not specify a remedy, so check for the visible gap and contact ICU Medical if concerned.
Look for the product name: 6.5 IN (17 cm) APPX 0.78 ml, EXT SET w/Clave CLEAR, Clave 4-WAY Stopcock, Spiros, RED CAP. The lot number 5782919 is associated with this recall.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1723-2022 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-1723-2022 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.
