Medical Device Recalls
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1 result found
Recall Number: Z-0804-2019 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Richard Wolf Bronchoscope Tubes, Model Texas. Device is reusable and should be sterilized prior to ... | 2 | 02/06/2019 |
FEI # 3002808001 Richard Wolf GmbH |
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