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
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-0446-2019 - -Outer Kit Box (P/N RFIT-LBL-0140) - FilmArray® Meningitis/Encephalitis (ME) Panel REF RFIT-ASY-0118 30 For FilmArray systems LOT KIT UDI (01)00815381020123 CE 0086 IVD -Fitment Label (P/N... | 2 | 11/10/2018 |
FEI # 3002773840 BioFire Diagnostics, LLC |
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