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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 189 Results
510(K) Number: K061573
 
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Product Description
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Triple Line SafeSet Kit with 03mL Flush Device, Item No. 46076-27 Product Usage: The Transpac ... 2 09/15/2016 FEI # 2025816
ICU Medical, Inc.
Trifurcated Transpac IV Monitoring Kit w/Safeset Reservoir, 03 ml Squeeze Flush and 6 Needleless Val... 2 08/07/2014 FEI # 2025816
ICU Medical, Inc.
Trifurcated Transpac IT Monitoring Kit w/03 ml Flush Devices, Needleless Valve and Macrodrip, Item N... 2 08/07/2014 FEI # 2025816
ICU Medical, Inc.
Trifurcated Monitoring Kit w/84" Safeset" Reservoir, TP4, 03 ml Squeeze Flush and Needleless Valve, ... 2 11/15/2016 FEI # 2025816
ICU Medical, Inc.
Transpac® w/Safeset Reservoir, Squeeze 03 ml Flush and Needleless Valve, Item No. 46101-82 The Tran... 2 11/15/2016 FEI # 2025816
ICU Medical, Inc.
Transpac® IV Trifurcated Monitoring Kit w/84" Safeset" Reservoir, 03 ml Squeeze Flush Device, Needle... 2 11/15/2016 FEI # 2025816
ICU Medical, Inc.
Transpac® IV Trifurcated Monitoring Kit w/03 ml Squeeze Flush Device, Arterial Safeset" Reservoir an... 2 11/15/2016 FEI # 2025816
ICU Medical, Inc.
Transpac® IV Trifurcated Monitoring Kit 84" w/03 ml Squeeze Flush Device, Red, Blue and Yellow Strip... 2 11/15/2016 FEI # 2025816
ICU Medical, Inc.
Transpac® IV Monitoring Kit, 84", Disposable Transducer, 3 ml Squeeze Flush, Macrodrip, Red Stripe P... 2 11/15/2016 FEI # 2025816
ICU Medical, Inc.
Transpac® IV Monitoring Kit, 84", Disposable Transducer, 3 ml Squeeze Flush, Macrodrip, Item No. 425... 2 11/15/2016 FEI # 2025816
ICU Medical, Inc.
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