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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 6 of 6 Results
Recall Date to: 08/23/2014 PMA Number: P880086
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Product Description
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FDA Recall
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Recalling Firm
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Implantable Pacemaker Accent DR models PM2110 and PM2210 St. Jude Medical pacemakers monitor and ... 2 01/11/2012 St Jude Medical CRMD
Anthem CRT-P models PM3110 and PM3210 St. Jude Medical pacemakers monitor and regulate a patient'... 2 01/11/2012 St Jude Medical CRMD
St. Jude Medical Identity SR Model 5172, Identity DR Model 5370, & Identity XL DR Model 5376; Pulse... 2 12/19/2006 St Jude Medical CRMD
St. Jude Medical APS III Programmer, used in combination with St. Jude Medical bradycardia and tachy... 2 12/19/2006 St Jude Medical CRMD
St. Jude Medical Merlin PCS Programmer, used in combination with St. Jude Medical bradycardia and ta... 2 12/19/2006 St Jude Medical CRMD
Pulse Generator 2 10/24/2003 St Jude Medical
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