ICU Medical recalls Sapphire Microbore Infusion Sets with Inline Filters due to potential fluid leakage from air vents. Affected units have specific product codes and lot numbers. Consumers should contact the company for details.
Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
ICU Medical is recalling specific Sapphire Microbore Infusion Sets with Inline Filters because they may leak fluid from air vents. This could cause issues with IV administration if not addressed.
Fluid leakage from air vents on the inline filters might cause IV fluids to leak outside the intended path. This could lead to improper medication delivery or contamination if not fixed.
Healthcare professionals using these infusion sets for IV administration are most at risk. Patients receiving IV treatments with the recalled sets could be affected.
Check for product codes 240130401 and lot numbers starting with 885585H or 925855H. The sets are labeled as SAPPHIRE Epidural Set with NRFit Connector Yellow-Striped Microbore, 0.2 Micron Filter, PAV, 123 Inch.
Look for product code 240130401 and lot numbers starting with 885585H or 925855H on the packaging.
The recalled sets are Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set with NRFit Connector Yellow-Striped Microbore, 0.2 Micron Filter, PAV, 123 Inch.
Check for product code 240130401 and lot numbers starting with 885585H or 925855H on the packaging.
The recall record does not specify a remedy, so contact ICU Medical directly for 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-0147-2020 — ICU Medical ICU Medical Hello, I own a ICU Medical that is covered by recall Z-0147-2020 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.
