Moog Medical recalls Curlin Infusion Administration Sets with particulate on spike. Affected units include specific model and serial numbers. Stop using immediately to prevent potential contamination.
Particulate found on the Curlin spike.
Moog Medical is recalling infusion sets that may have particulate in the spike. This could lead to contamination if used for medical administration. Affected units have specific model numbers and serial codes.
Particulate matter found on the spike can contaminate the fluid being administered. This poses a risk of infection or adverse reactions in patients receiving intravenous or other medical infusions.
Healthcare professionals using the Moog Curlin Infusion Pump system with the recalled sets. Patients receiving infusions through these devices are at risk if the particulate contaminates the fluid.
Check for model number 340-4166 and serial numbers CF1515305 through CF1614732. The product was sold with the Moog Curlin Ambulatory Volumetric Infusion Pump.
Discontinue use of the affected infusion sets to prevent potential contamination.
The model number is 340-4166.
Affected serial numbers include CF1515305, CF1519505, CF1523004, CF1524405, CF1529201, CF1528602, CF1532105, CF1601204, CF1604701, CF1605403, CF1609005, CF1609604, and CF1614732.
The recall record does not mention a remedy or replacement option.
We’ve drafted a message you can send Moog Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0700-2018 — Moog Medical Moog Medical Hello, I own a Moog Medical that is covered by recall Z-0700-2018 from Moog 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.
