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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 56 Results
510(K) Number: K981816
 
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Model 6000 CMS, CMS IOD, or Plus Ambulatory Infusion Pump, Model Number: 360-1101 2 09/22/2008 FEI # 3002936294
Curlin Medical Llc
Model 4000 CMS Ambulatory Infusion Pump, Model Number: 350-1101 2 09/22/2008 FEI # 3002936294
Curlin Medical Llc
Model 4000 Plus Ambulatory Infusion Pump, Model Number: 350-1001 2 09/22/2008 FEI # 3002936294
Curlin Medical Llc
Model 2000 CMS/ Model 2000 Plus Ambulatory Infusion Pump, Model Number: 340-1001 2 09/22/2008 FEI # 3002936294
Curlin Medical Llc
PainSmart, PainSmart IOD Ambulatory Infusion System, Model Number: 360-1301 2 09/22/2008 FEI # 3002936294
Curlin Medical Llc
Curlin Medical Administration Sets: Model Numbers 340-4111, IV Administration Sets. 2 08/07/2007 FEI # 3002936294
Curlin Medical Llc
Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusion System includes Curl... 2 02/11/2016 FEI # 1000117172
MOOG Medical Devices Group
***This recall is being conducted due to an incomplete recall for RES 57829*** Curlin Infusion Admin... 2 10/17/2012 FEI # 1000117172
MOOG Medical Devices Group
Non-DEHP Epidural Admin Set with 0.2 Micron Filter Non-Vented Bag Spike ASV Packaged, product code: ... 1 05/30/2012 FEI # 1000117172
MOOG Medical Devices Group
Non-DEHP Microbore Administration Set with Non-Vented Spike ASV Packaged, product code: 340-4166, Me... 1 05/30/2012 FEI # 1000117172
MOOG Medical Devices Group
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