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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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PainSmart, PainSmart IOD Ambulatory Infusion System, Model Number: 360-1301 2 09/22/2008 Curlin Medical Llc
Non-DEHP Microbore Administrative Set with Female Luer Adapter Packaged Assembly, product code: 340-... 1 05/30/2012 MOOG Medical Devices Group
Non-DEHP Microbore Administrative Set with Female Luer Adapter Packaged Assembly, product code: 340-... 1 05/30/2012 MOOG Medical Devices Group
Non-DEHP Microbore Administration Set with Non-Vented Spike Packaged Assembly, product code: 340-411... 1 05/30/2012 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
Non-DEHP Microbore Administration Set with Non-Vented Spike ASV Packaged, product code: 340-4166, Me... 1 05/30/2012 MOOG Medical Devices Group
Non-DEHP Microbore Admin Set with Non-Vented Spike and Needleless Injection Port Positive Pressure P... 1 05/30/2012 MOOG Medical Devices Group
Non-DEHP Microbore Admin Set with Female Male Luer Locks and Y-Site with Check Valve Packaged Assemb... 1 05/30/2012 MOOG Medical Devices Group
Non-DEHP Epidural Yellow Striped Tubing Admin Set with Vented Vial Spike and 0.2 Micron Filter Packa... 1 05/30/2012 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 MOOG Medical Devices Group
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