Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K042076 |
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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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Endoscope; ED-530XT Operation Manual 'Operation and Preparation' and 'Cleaning, Disinfection and St... | 2 | 05/31/2016 | Fujifilm Medical Systems U.S.A., Inc. |
Endoscope ED-450XL5 Operation Manual: Cleaning, Disinfection and Storage | 2 | 05/31/2016 | Fujifilm Medical Systems U.S.A., Inc. |
Endoscope ED-450XT5 Operation Manual: Cleaning, Disinfection and Storage | 2 | 05/31/2016 | Fujifilm Medical Systems U.S.A., Inc. |
Fujifilm Medical Endoscope for the duodenum and upper G.I. tract. ED-530XT, ED-250XT5, ED-250XL5, E... | 2 | 09/17/2015 | Fujifilm Medical Systems U.S.A., Inc. |
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