Moog Medical recalls Curlin Infusion Administration Sets with particulate in spike. Stop using if you have model 340-4168 with specific serial numbers to avoid potential contamination.
Particulate found on the Curlin spike.
Moog Medical is recalling infusion sets that may contain particles in the spike. This could lead to contamination if used for medical infusions, posing a risk to patients.
The spike (the part that connects to the patient) may have particles that could enter the bloodstream during infusion. This could cause infection or other complications if the particles are not properly filtered.
Patients using the Moog Curlin infusion pump with this specific model and serial numbers are most at risk. Healthcare providers administering these sets should check if they have the recalled units.
Check for the model number 340-4168 on the packaging. The serial numbers listed include CF1517404, CF1519506, CF1521211, and others. These units were sold with the Moog Curlin Ambulatory Volumetric Infusion Pump.
Look for the model number 340-4168 and the listed serial numbers on the packaging or label.
If you have the recalled model and serial numbers, stop using the infusion set immediately to avoid potential contamination.
The model number is 340-4168 for the Moog Curlin Infusion Administration Set.
The affected serial numbers include CF1517404, CF1519506, CF1521211, CF1522501, CF1526503, CF1530704, and CF1611001.
The recall record does not specify a return process or remedy, so you should contact Moog Medical directly for further instructions.
We’ve drafted a message you can send Moog Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0701-2018 — Moog Medical Moog Medical Hello, I own a Moog Medical that is covered by recall Z-0701-2018 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.
