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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 15 of 15 Results
510(K) Number: K942988
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Product Description
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Recall
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FDA Recall
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Outlook Pump IV Set w/Universal Spike, 2 Safesite Inj sites, 0.2um Filter, Pressure limited check va... 2 01/26/2010 B. Braun Medical, Inc.
Outlook Pump IV Set w/Universal Spike, 2 Ultrasite Inj sites, 0.2um Filter, Pressure limited check v... 2 01/26/2010 B. Braun Medical, Inc.
Outlook® Pump 15 Drop 0.2 Micron Filtered IV Set with 2 CARESITE® Y-Sites: single-use for use with t... 2 09/24/2021 B. Braun Medical, Inc.
SAFSITE® Injection Sites and IV Sets manufactured with SAFSITE® Injection Sites. A device used to... 2 02/18/2014 B. Braun Medical, Inc.
STOPCOCK EXT. SET W/ 3-WAY STOPCOCK WITH INJ. SITE AND SPINLOCK CONNECTOR, 22 inches and 37 inches 2 07/09/2014 B. Braun Medical, Inc.
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