Medical Device Recalls
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1 result found
PMA Number: P820003/S072 |
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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 Dual Chamber Temporary Pacemaker, model 5388. Manufacturer: Medtronic, Inc., 710 Medtron... | 2 | 11/22/2010 | Medtronic Inc. Cardiac Rhythm Disease Managment |
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