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U.S. Department of Health and Human Services

Medical Device Recalls
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101 to 110 of 301 Results
Product: pacemaker
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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Model Number L231, PROPONENT DR EL 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 L211 PROPONENT DR SL MRI Pacemaker 1 10/10/2025 Boston Scientific Corporation
Model Number L210 PROPONENT SR SL Pacemaker 1 10/10/2025 Boston Scientific Corporation
Model Number L209 PROPONENT DR (VDD) SL Pacemaker 1 10/10/2025 Boston Scientific Corporation
Model Number L131, ESSENTIO DR EL MRI Pacemaker 1 10/10/2025 Boston Scientific Corporation
Model Number L121 ESSENTIO DR EL Pacemaker 1 10/10/2025 Boston Scientific Corporation
Model Number L111, ESSENTIO DR SL MRI Pacemaker 1 10/10/2025 Boston Scientific Corporation
Model Number L110, ESSENTIO SR SL MRI Pacemaker 1 10/10/2025 Boston Scientific Corporation
Model Number L101, ESSENTIO DR SL Pacemaker 1 10/10/2025 Boston Scientific Corporation
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