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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 23 Results
Related Medical Device Recalls
 
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Product Description
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FDA Recall
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Z-0067-2026 - OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40 1 10/16/2025 Olympus Corporation of the Americas
Z-0058-2026 - OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60 1 10/16/2025 Olympus Corporation of the Americas
Z-0054-2026 - OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE MP60 1 10/16/2025 Olympus Corporation of the Americas
Z-0047-2026 - OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60 1 10/16/2025 Olympus Corporation of the Americas
Z-0066-2026 - EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS BF-XT190 1 10/16/2025 Olympus Corporation of the Americas
Z-0063-2026 - EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190 1 10/16/2025 Olympus Corporation of the Americas
Z-0057-2026 - EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190 1 10/16/2025 Olympus Corporation of the Americas
Z-0053-2026 - EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-H190 1 10/16/2025 Olympus Corporation of the Americas
Z-0049-2026 - EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-1TH190 1 10/16/2025 Olympus Corporation of the Americas
Z-0062-2026 - EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180-AC 1 10/16/2025 Olympus Corporation of the Americas
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