Moog Medical recalls Curlin Infusion Administration Sets with particulate in the spike, which could cause blockages or infections during IV treatments. Affected units include specific model numbers and batch dates.
Particulate found on the Curlin spike.
Moog Medical is recalling its Curlin Infusion Administration Sets due to a risk of particulate matter in the spike, which could cause blockages or infections during IV treatments. This affects specific model numbers and batch dates sold to healthcare providers.
The spike (the part that connects the IV bag to the patient) may contain small particles that could clog the tubing or cause infections when used for intravenous treatments. This is a potential risk during IV administration but does not typically cause serious injury in normal use.
Healthcare providers using the Moog Curlin Ambulatory Volumetric Infusion Pump system are most at risk. Patients receiving IV treatments with this specific product may be affected if the spike contains particulate matter.
Check for the product name 'MOOG Curlin Infusion Administration Set, Ref 340-4114' with non-DEHP microbore tubing and non-vented bag spike. Look for specific batch numbers listed in the recall, such as CF1514701 to CF1616608.
Verify the product name, model number (340-4114), and batch numbers listed in the recall to confirm if your unit is affected.
The recall is due to particulate matter found on the spike, which could potentially cause blockages or infections during intravenous treatments.
Check the product details and batch numbers against the list provided in the recall to determine if your unit is affected. If affected, contact Moog Medical for further instructions.
The recall record does not specify a remedy or fix for this issue.
We’ve drafted a message you can send Moog Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0697-2018 — Moog Medical Moog Medical Hello, I own a Moog Medical that is covered by recall Z-0697-2018 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.
