Moog Medical recalls Curlin Infusion Administration Sets with particulate in spike. Stop using if you have model 340-413: 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 cause contamination during IV treatments, making it unsafe for medical use.
Particulate matter in the spike can enter the bloodstream during IV infusions. This may cause infections or other complications if the particles are not properly filtered.
Patients using Moog Curlin infusion pumps with this specific set model are affected. Healthcare providers administering IV treatments with these sets face the highest risk.
Check for model number 340-4134 on the packaging. The product was sold with lot numbers CF1518304, CF1521104, CF1524301, CF1523803, CF1528603, and CF1613101.
If you have the model 340-4134 set with listed lot numbers, stop using it immediately to avoid contamination.
Yes, the recall states particulate matter in the spike could cause contamination during IV infusions.
Check the model number and lot numbers listed. If you have the recalled set, stop using it immediately.
Look for model 340-4134 on the packaging and check if your lot number matches CF1518304, CF1521104, CF1524301, CF1523803, CF1528603, or CF1613101.
We’ve drafted a message you can send Moog Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0699-2018 — Moog Medical Moog Medical Hello, I own a Moog Medical that is covered by recall Z-0699-2018 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.
