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MOOG Medical Devices Group Recalls
5 recalls on record · October 24, 2012 to February 17, 2016 · Medical Devices
Recalls by year
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16
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 17, 2016Medical DevicesFDA
MOOG Medical Devices Group recalls Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusion System includes Curlin Ambulatory multi-
Hazard: 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.
December 23, 2015Medical DevicesFDA
MOOG Medical Devices Group recalls Catalog No. INF0020-A EnteraLite Infinity Enteral Pump Delivery Set with ENFit Connector System and Transitional Stepp
Hazard: Potential for leaking between the purple ENFit connector and the white transitional stepped connector due to cracking or breaking of the purple connector.
February 6, 2013Medical DevicesFDA
MOOG Medical Devices Group recalls Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum to Operator's Manual Product usage: pr
Hazard: The firm is adding an addendum to the operator's manual for Infinity Enteralite Ambulatory Feeding Pumps pertaining to the Infinite Dose mode and the inability of the Pump to detect air in line.
November 21, 2012Medical DevicesFDA
MOOG Medical Devices Group recalls EnteraLite Infinity Enteral Feeding Pump identified with the following list numbers: INFKIT2 and INFORNG. The device is
Hazard: MOOG Medical Devices Group is conducting a voluntary for a limited set of serial numbers of the EnteraLite Infinity and Infinity Orange Small Volume Enteral Feeding Pumps because certain diodes on the PCB assembly may result in insufficient voltage to a portion of the pump resulting in an error 13 message and shutting the pump down entirely.
October 24, 2012Medical DevicesFDA
MOOG Medical Devices Group recalls ***This recall is being conducted due to an incomplete recall for RES 57829*** Curlin Infusion Administration Set, REF 3
Hazard: This recall is the same issue for the FDA processed recall initiated by Moog Medical Devices on 1/25/11 which was related to customers reporting unclearable Air-In-Line alarm with specific lot numbers of Curlin Administration Sets used with Curlin Ambulatory Infusion Pumps. The lots associated with this recall were inadvertently omitted from the original recall which has since been terminated by