Medical Device Recalls
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1 result found
510(K) Number: K984535 |
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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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Puritan Bennett 840 ventilator systems software part number 4-070212-85, revision AB-AG. The inte... | 1 | 01/03/2014 | Covidien |
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