MOOG recalls 20-set infusion sets with leaking filter that could cause contamination. Stop using if you have model REF 340-4130, lots CF1819415-23615.
Administration sets leaked at the filter.
MOOG is recalling infusion sets that leak at the filter. This could lead to contaminated medication being administered, which is dangerous for patients.
The filter in the infusion set leaks, allowing medication to mix with contaminants. This could cause infection or other complications if the contaminated solution enters the bloodstream.
Patients using the MOOG Curlin Infusion Pump with this specific set are at risk. Healthcare providers and patients receiving IV treatments are most affected.
Check for the model number REF 340-4130 on the packaging. The product was sold in cartons of 20 sets with lot numbers CF1819415, CF1820215, CF1821616, CF1822914, or CF1823615.
Look for the model number REF 340-4130 and lot numbers CF1819415 through CF1823615 on the packaging.
The filter in the infusion set leaks, which could lead to contaminated medication being administered to patients.
Check for the model number REF 340-4130 and lot numbers CF1819415, CF1820215, CF1821616, CF1822914, or CF1823615 on the packaging.
The recall record does not specify a remedy, so contact MOOG Medical Devices for guidance.
We’ve drafted a message you can send MOOG Medical Devices to request your refund or repair — edit it as you like.
Subject: Recall Z-2053-2019 — MOOG Medical Devices MOOG Medical Devices Hello, I own a MOOG Medical Devices that is covered by recall Z-2053-2019 from MOOG Medical Devices. 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.
