ICU Medical recalls 7-inch small bore IV sets with incorrect filter assembly that could cause improper fluid administration during medical procedures.
Due to the incorrect filter assembly.
ICU Medical is recalling small bore IV sets that have an incorrect filter assembly. This could lead to improper fluid administration during medical procedures, potentially causing harm to patients.
The incorrect filter assembly in the IV set could lead to improper fluid administration during medical procedures. This might cause complications for patients receiving intravenous treatments.
Healthcare professionals using these IV sets for patient care are most at risk. Patients receiving intravenous treatments with these sets could be affected.
Check for the model number Z3532 on the packaging or label. The product is a small bore IV set used for intravascular administration.
Look for the model number Z3532 and lot number 4795091 on the packaging or label.
The incorrect filter assembly could lead to improper fluid administration during medical procedures.
Check for the model number Z3532 and lot number 4795091 on the packaging or label.
The recall record does not specify a remedy, so contact ICU Medical directly for guidance.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0957-2021 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-0957-2021 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.
