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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K932188
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Product Description
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Monitoring Kit with 03mL Flush Device, Item No. 46080-57 Product Usage: The Transpac Disposable... 2 09/15/2016 FEI # 2025816
ICU Medical, Inc.
Monitoring Kit with TP4, 30 ml Squeeze Flush Device, 10 cc Contamination Syringe and Needleless Valv... 2 09/15/2016 FEI # 2025816
ICU Medical, Inc.
5 Port OFF Manifold with Transpac IV, Item No. 46100-29 Usage: The Transpac Disposable Straigh... 2 09/15/2016 FEI # 2025816
ICU Medical, Inc.
Bifurcated SafeSet Kit with 03mL Flush Device, Item No. 46091-75 Product Usage: The Transpac D... 2 09/15/2016 FEI # 2025816
ICU Medical, Inc.
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