Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K152864 |
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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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Fellows "Mighty 8" Power strip (Part Number 04175-0008) and TrippLite Power strip (PS-415-HGULTRA - ... | 2 | 01/14/2018 | Merge Healthcare, Inc. |
Merge Hemo, Software packages 10.2, 10.3, and 10.4 | 2 | 08/28/2021 | Merge Healthcare, Inc. |
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