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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: 10/25/2014
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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-1659-2012 - Non-DEHP Microbore Administration Set with Non-Vented Spike Packaged Assembly, product code: 340-4114, Method of Sterilization using Ethylene Oxide. The Curlin® Ambulatory Infusion Pump System with... 1 05/30/2012 MOOG Medical Devices Group
Z-1660-2012 - Non-DEHP Microbore Administrative Set with Female Luer Adapter Packaged Assembly, product code: 340-4115, Method of Sterilization using Ethylene Oxide. The Curlin® Ambulatory Infusion Pump System w... 1 05/30/2012 MOOG Medical Devices Group
Z-1672-2012 - Non-DEHP Microbore Administrative Set with Female Luer Adapter Packaged Assembly, product code: 340-4176, Method of Sterilization using Ethylene Oxide. The Curlin® Ambulatory Infusion Pump System w... 1 05/30/2012 MOOG Medical Devices Group
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