Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Moog Curlin Infusion Recalled by MOOG Medical Devices Group Due to Moog is recalling Curlin 4000, 6000, and PainSmart...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact MOOG Medical Devices Group directly.
Affected Products
Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusion System includes Curlin Ambulatory multi-therapy and PainSmart pumps. Curlin 4000, catalog number 340; Curlin 6000, 6000 CMS, and PainSmart IOD, catalog number 360; and Curlin Pump Calibration Set, catalog number 340-4038.
Quantity: 11,472
Why Was This Recalled?
Moog is recalling Curlin 4000, 6000, and PainSmart Infusion Pumps manufactured or serviced by MMDG between March 18, 2015 and November 6, 2015 because the master pumps used to calibrate them were out of tolerance and may cause an over delivery of medications and solutions at a rate of 1.2 - 6.8% faster than programmed.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About MOOG Medical Devices Group
MOOG Medical Devices Group has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report