Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K210743 |
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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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ACUSON Redwood 1.0 Diagnostic Ultrasound System, REF: 11503314, running software version VA10A to VA... | 2 | 04/19/2024 | Siemens Medical Solutions USA, Inc. |
ACUSON Redwood 2.0 ultrasound systems, REF: 11503314 | 2 | 09/13/2023 | Siemens Medical Solutions USA, Inc. |
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