Medical Device Recalls
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1 to 3 of 3 Results
Recall Date to: 08/29/2014 PMA Number: P980035/S002 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Medtronic SIGMA 100/200/300 Series IPGs, Single Chamber Pacemaker; models SS103, SS106, SS203, and S... | 1 | 06/11/2009 | Medtronic Inc. Cardiac Rhythm Disease Managment |
Medtronic SIGMA 100/200/300 Series IPGs, Dual Chamber atrial sensing, ventricular sensing and pacing... | 1 | 06/11/2009 | Medtronic Inc. Cardiac Rhythm Disease Managment |
Medtronic SIGMA 100/200/300 Series IPGs, Dual Chamber Pacemaker, models SD203 and SD303. | 1 | 06/11/2009 | Medtronic Inc. Cardiac Rhythm Disease Managment |
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