Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K090318 |
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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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CARESTREAM DRX -Mobile Retrofit Kit, Catalog number: 1019397. Made in U.S.A. by Carestream Health, ... | 2 | 11/07/2013 | Carestream Health Inc. |
Carestream DRX-1 System Battery --- Made in U.S.A. for Carestream Health, Inc., Carestream Health, I... | 2 | 08/13/2012 | Carestream Health, Inc. |
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