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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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Non-DEHP Admin Set with Non-Vented Spike and 1.2 Micron Filter Packaged Assembly, product code: 340-... 1 05/30/2012 FEI # 1000117172
MOOG Medical Devices Group
Non-DEHP Microbore Admin Set with Non-Vented Spike and Needleless Injection Port Positive Pressure P... 1 05/30/2012 FEI # 1000117172
MOOG Medical Devices Group
Non-DEHP Admin Set Non-Vented Spike and 1.2 Micron Filter ASV Packaged Assembly, product code: 340-4... 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
Non-DEHP Microbore Administration Set with Non-Vented Spike Packaged Assembly, product code: 340-411... 1 05/30/2012 FEI # 1000117172
MOOG Medical Devices Group
Non-DEHP Microbore Administrative Set with Female Luer Adapter Packaged Assembly, product code: 340-... 1 05/30/2012 FEI # 1000117172
MOOG Medical Devices Group
Epidural Admin Set with Non-Vented Bag Spike and 0.2 Micron Filter Package Assembly, product code: 3... 1 05/30/2012 FEI # 1000117172
MOOG Medical Devices Group
Non-DEHP Admin Set with Non-Vented Spike and 1.2 Micron Filter Packaged Assembly, product code: 340-... 1 05/30/2012 FEI # 1000117172
MOOG Medical Devices Group
Non-DEHP Microbore Administrative Set with Female Luer Adapter Packaged Assembly, product code: 340-... 1 05/30/2012 FEI # 1000117172
MOOG Medical Devices Group
Non-DEHP Admin Set with Non-Vented Spike and 0.2 Micron Filter Packaged Assembly, product code: 340-... 1 05/30/2012 FEI # 1000117172
MOOG Medical Devices Group
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