Moog Medical recalls Curlin Infusion Administration Sets with particulate in spike. Stop using if you have model 340-416: risk of contamination during IV infusions.
Particulate found on the Curlin spike.
Moog Medical is recalling infusion sets that may have particles in the spike. This could lead to contamination during IV treatments, which is a serious risk for patients receiving infusions.
Particles in the spike can enter the bloodstream during IV infusions, potentially causing infections or other complications. This is a serious hazard because the spike is directly connected to the patient's bloodstream.
Patients using the Moog Curlin infusion pump with this specific model set. Those with the model number 340-4169 are most at risk.
Look for the model number 340-4169 on the packaging. The sets were sold with lot numbers CF1520208, CF1522301, or CF1532971. They come in packs of 20 per box.
Immediately stop using the infusion set if you have the model number 340-4169.
No, this recall is specific to the Curlin Infusion Administration Set model 340-4169 with particulate in the spike.
Check the model number on the packaging; affected sets have model 340-4169 and lot numbers CF1520208, CF1522301, or CF1532971.
Stop using it immediately and contact Moog Medical for instructions on replacement.
We’ve drafted a message you can send Moog Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0702-2018 — Moog Medical Moog Medical Hello, I own a Moog Medical that is covered by recall Z-0702-2018 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.
