Medical Device Recalls
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1 result found
Recall Number: Z-2049-2026 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| LUX-Dx II Plus, Arrythmia detector and alarm, Model M312, with SERVER SW LATITUDE DRAGON EU (Europe)... | 2 | 05/01/2026 |
FEI # 2124215 Boston Scientific Corporation |
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