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U.S. Department of Health and Human Services

Medical Device Recalls

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11 to 20 of 185 Results
510(K) Number: K964435
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Product Description
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Class
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FDA Recall
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127" (323cm) Transfer Set w/Check Valve, MicroClave T-Connector, Anti-Siphon Valve, Clamp, Luer Lock... 2 05/07/2015 ICU Medical, Inc.
98" (249 cm) Transfer Set w/MicroClave T-Connector, Check Valve, Anti-Siphon Valve, Trifuse Ext Set ... 2 05/07/2015 ICU Medical, Inc.
113" (287cm) Transfer Set w/MicroClave T-Connector, Check Valve, Anti-Siphon Valve, Smallbore Quadfu... 2 05/07/2015 ICU Medical, Inc.
133" 60 Drop 24 Hour Primary Set w/2 Bravo24®, 2 Gang 1o2® Manifold, Rotating Luer, 1 Ext, Item No. ... 2 01/10/2017 ICU Medical, Inc.
168 cm (66") Appx 2.6 ml, PVC/PUR Smallbore Ext Set w/6-Port NanoClave® Manifold, Check Valve, Micro... 2 06/26/2017 ICU Medical, Inc.
28 cm (11") PUR Bifuse Ext Set w/6-Port NanoClave® Manifold, Check Valve, 2 NanoClave®, Rotating Lue... 2 06/26/2017 ICU Medical, Inc.
28 cm (11") PUR Smallbore Ext Set w/6-Port NanoClave® Manifold, Check Valve, NanoClave®, Rotating Lu... 2 06/26/2017 ICU Medical, Inc.
18 cm (7") PUR Smallbore Ext Set w/6-Port NanoClave® Manifold, Check Valve, NanoClave®, Rotating Lue... 2 06/26/2017 ICU Medical, Inc.
PROXIMALE - 28 cm (11") Smallbore Ext Set w/6-Port NanoClave® Manifold, Check Valve, NanoClave® (Red... 2 06/26/2017 ICU Medical, Inc.
Kit w/3 Ext Sets, 3 Drop-In MicroClave® Clear. Product Usage: The device is a single use, sterile,... 2 06/26/2017 ICU Medical, Inc.
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