Medical Device Recalls
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1 to 10 of 30 Results
Product Code: eoq Recall Date from: 07/01/2018 Recall Date to: 12/01/2018 Firm: olympus |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Airway Mobilescope MAF-TM | 2 | 09/29/2018 | Olympus Corporation of the Americas |
Bronchofibercope BF-6C240 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
Bronchofiberscope BF-40 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
Bronchofiberscope BF-P40 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
Bronchofiberscope BF-P60 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
Bronchofiberscope BF-XP40 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
Bronchofiberscope BF-XP60 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
Bronchofiberscope BF-XT40 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
Bronchofiberscope F-1T160 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
Bronchovideoscope BF-160 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
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