Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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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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Z-1203-2017 - The Schiller PB 1000, also known as: Merge Hemo Patient Data Module (PDM), V2 model, a major component of the Merge Hemo software. | 2 | 02/15/2017 | Merge Healthcare, Inc. |
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