Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
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FDA Recall
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Z-0877-2017 - BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath® Preservative Fluid is designed for use with the PrepStain® System. SurePath® Pres... | 2 | 12/21/2016 | Becton Dickinson & Co. |
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