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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 of 56 Results
510(K) Number: K981816
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MOOG Curlin Infusion Administration Set, Ref 340-4114, Non-DEHP Microbore Tubing with Non-Vented Bag... 2 02/23/2018 Zevex Incorporated (dba Moog Medical Medical Devices Group)
MOOG Curlin Infusion Administration Set, Ref 340-4134, Non-DEHP Microbore Tubing with Non-Vented Bag... 2 02/23/2018 Zevex Incorporated (dba Moog Medical Medical Devices Group)
MOOG Curlin Infusion Administration Set, Ref 340-4166, Non-DEHP Microbore Tubing with Non-Vented Spi... 2 02/23/2018 Zevex Incorporated (dba Moog Medical Medical Devices Group)
MOOG Curlin Infusion Administration Set, Ref 340-4168, Non-DEHP Microbore Tubing with Non-Vented Bag... 2 02/23/2018 Zevex Incorporated (dba Moog Medical Medical Devices Group)
MOOG Curlin Infusion Administration Set, Ref 340-4169, Non-DEHP Microbore Tubing with Non-Vented Bag... 2 02/23/2018 Zevex Incorporated (dba Moog Medical Medical Devices Group)
MOOG Curlin Infusion Administration Set, Ref 340-4133, Non-DEHP Microbore Tubing with Non-Vented Bag... 2 02/23/2018 Zevex Incorporated (dba Moog Medical Medical Devices Group)
Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusion System includes Curl... 2 02/11/2016 MOOG Medical Devices Group
***This recall is being conducted due to an incomplete recall for RES 57829*** Curlin Infusion Admin... 2 10/17/2012 MOOG Medical Devices Group
Non-DEHP Microbore Administration Set with Non-Vented Spike Packaged Assembly The Curlin Ambulato... 2 04/13/2012 MOOG Medical Devices Group
Curlin Infusion Administration Set, REF 340-4114, Sterile EO, Zevex, Inc., 4314 Zevex Park Lane, Sal... 2 02/25/2011 Zevex International, Inc.
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