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U.S. Department of Health and Human Services

Medical Device Recalls
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81 to 90 of 284 Results
Product: pacemaker
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PULSAR and PULSAR MAX (model nos. 470, 870, 970, 972, 1170, 1171, 1172, 1270 and 1272) pacemaker. S... 1 07/28/2005 Guidant Corporation
PULSAR MAX II (model nos. 1180, 1181 and 1280) pacemaker. Sterilized with gaseous ethylene oxide. ... 1 07/28/2005 Guidant Corporation
PSW 1203.U/1, PSW 1301.U, PSW 1307.U, PSW 1403.U, and PSW 1501.U Pacemaker Programmer software. Sof... 2 08/13/2015 BIOTRONIK, Inc.
PROPONENT VDD SL Pacemaker 2 01/15/2018 Boston Scientific Corporation
PROPONENT SR Pacemaker 2 01/15/2018 Boston Scientific Corporation
PROPONENT Pacemaker 2 09/27/2018 Boston Scientific Corporation
PROPONENT MRI Pacemaker 2 01/15/2018 Boston Scientific Corporation
PROPONENT EL DR Pacemaker 2 01/15/2018 Boston Scientific Corporation
PROPONENT DR Pacemaker, SL (Model Number L201), (VDD) SL (Model Number L209), SL MRI (Model Number L... 1 01/10/2025 Boston Scientific Corporation
PROPONENT DR Pacemaker 2 01/15/2018 Boston Scientific Corporation
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