Medical Device Recalls
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61 to 61 of 61 Results
Recall Date to: 04/20/2014 PMA Number: P860004 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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8870 software application card versions AAA 02, BBB 04, BBC 02, and BBD 01, which is used in conjunc... | 1 | 09/23/2004 | Medtronic Inc, Neurological & Spinal Division |
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