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U.S. Department of Health and Human Services

Medical Device Recalls
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71 to 80 of 500 Results *
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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PROPONENT SR SL (Model L200) 1 10/10/2025 Boston Scientific Corporation
PROPONENT DR SL (Model L201) 1 10/10/2025 Boston Scientific Corporation
Model Number L209 PROPONENT DR (VDD) SL Pacemaker 1 10/10/2025 Boston Scientific Corporation
Model Number L210 PROPONENT SR SL Pacemaker 1 10/10/2025 Boston Scientific Corporation
Model Number L211 PROPONENT DR SL MRI Pacemaker 1 10/10/2025 Boston Scientific Corporation
Model Number L221 PROPONENT DR EL Pacemaker 1 10/10/2025 Boston Scientific Corporation
Model Number L231, PROPONENT DR EL MRI Pacemaker 1 10/10/2025 Boston Scientific Corporation
Model Number L100, ESSENTIO SR SL Pacemaker 1 10/10/2025 Boston Scientific Corporation
Model Number L101, ESSENTIO DR SL Pacemaker 1 10/10/2025 Boston Scientific Corporation
Model Number L110, ESSENTIO SR SL MRI Pacemaker 1 10/10/2025 Boston Scientific Corporation

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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