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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K212656
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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Five S 5 3x65, REF: 0915612-06, sterile for single use, Sterile EO, Rx Only 2 09/15/2023 Karl Storz Endoscopy
11005BC1 11005BCK1 Flexible Bronchoscope Z21493US-BA (06/2019) 2 05/10/2022 Karl Storz Endoscopy
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