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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: K954123
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Product Description
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FDA Recall
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Extension Set, EXT SET W/CARESITE, 6IN., Product Code 470169, 50 units per carton. A6 Access Device ... 2 10/14/2022 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.
Outlook Pump IV Set with Universal Spike, Check Valve, 3 Safeline Inj Sites, B/C Valve, Spin Lock Co... 2 01/26/2010 B. Braun Medical, Inc.
Safesite Y Type Blood Set for Outlook Pump w/Safesite Inj Site 170um Blood Filter, Spin Lock Connect... 2 01/26/2010 B. Braun Medical, Inc.
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