ICU Medical recalls Plum Microbore Infusion Sets with inline filters due to potential fluid leakage from air vents. Affected units sold outside the U.S. with specific product codes.
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
ICU Medical is recalling Plum Microbore Infusion Sets with inline filters because fluid may leak from air vents. This could cause issues with IV administration if not addressed.
Fluid leakage from air vents on inline filters could lead to improper IV administration. This might cause incorrect fluid delivery or contamination risks during medical procedures.
Healthcare professionals using IV pumps in medical settings may be affected. Patients receiving IV treatments with these specific sets are at risk.
Check for Plum Microbore Infusion Sets with inline filters labeled as Primary. Look for product codes like 140099290 or lot numbers starting with 855575H.
Identify if your set has the specific product codes or lot numbers listed in the recall notice.
No, these sets were not distributed in the U.S. as stated in the recall record.
The recall record does not specify a remedy, so contact ICU Medical directly for guidance.
Look for product codes like 140099290 or lot numbers starting with 855575H on the packaging.
We’ve drafted a message you can send ICU Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0137-2020 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-0137-2020 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.
