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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 14 of 14 Results
Related Medical Device Recalls Recall Date to: 09/01/2014
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Product Description
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Z-1669-2012 - Non-DEHP Microbore Administration Set with Non-Vented Spike ASV Packaged, product code: 340-4166, Method of Sterilization using Ethylene Oxide. The Curlin® Ambulatory Infusion Pump System with disp... 1 05/30/2012 MOOG Medical Devices Group
Z-1670-2012 - Non-DEHP Admin Set Non-Vented Spike and 1.2 Micron Filter ASV Packaged Assembly, product code: 340-4173, Method of Sterilization using Ethylene Oxide. The Curlin® Ambulatory Infusion Pump System wi... 1 05/30/2012 MOOG Medical Devices Group
Z-1671-2012 - Non-DEHP Microbore Admin Set with Non-Vented Spike and Needleless Injection Port Positive Pressure Package Assembly, product code: 340-4133, Method of Sterilization using Ethylene Oxide. The Curlin... 1 05/30/2012 MOOG Medical Devices Group
Z-1665-2012 - Non-DEHP Admin Set with Non-Vented Spike and 0.2 Micron Filter Packaged Assembly, product code: 340-4130-V, Method of Sterilization using Ethylene Oxide. The Curlin® Ambulatory Infusion Pump System... 1 05/30/2012 MOOG Medical Devices Group
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