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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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Recall
Class
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FDA Recall
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Z-0059-2026 - BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2 1 10/16/2025 Olympus Corporation of the Americas
Z-0064-2026 - BRONCHOFIBERSCOPE OLYMPUS BF TYPE TE2 1 10/16/2025 Olympus Corporation of the Americas
Z-0045-2026 - BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 1 10/16/2025 Olympus Corporation of the Americas
Z-0055-2026 - BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P150 1 10/16/2025 Olympus Corporation of the Americas
Z-0048-2026 - BRONCHOVIDEOSCOPE OLYMPUS BF-1TH1100 1 10/16/2025 Olympus Corporation of the Americas
Z-0050-2026 - BRONCHOVIDEOSCOPE OLYMPUS BF-1TQ170 1 10/16/2025 Olympus Corporation of the Americas
Z-0052-2026 - BRONCHOVIDEOSCOPE OLYMPUS BF-H1100 1 10/16/2025 Olympus Corporation of the Americas
Z-0060-2026 - BRONCHOVIDEOSCOPE OLYMPUS BF-Q170 1 10/16/2025 Olympus Corporation of the Americas
Z-0065-2026 - EVIS EXERA BRONCHOVIDEOSCOPE OLYMPUS BF TYPE XT160 1 10/16/2025 Olympus Corporation of the Americas
Z-0046-2026 - EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T180 1 10/16/2025 Olympus Corporation of the Americas
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