Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K954123 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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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