FDA•MODERATE
VITEK 2 Gram-negative Susceptibility Cards
Biomerieux is recalling 30+ VITEK 2 susceptibility cards due to potential quality control failures and false resistant test results.
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Medical Devices Recalls
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FDA•MODERATEPrismaflex M100 SetVantive is recalling the Prismaflex M100 Set due to a potential dislodgement of the deaeration chamber from the control unit.
8 products
FDA•MODERATEEncore Medical EMPOWR Acetabular and Knee InsertsEncore Medical is recalling EMPOWR acetabular liners and knee inserts due to a packaging discrepancy that may cause surgical delays.
2 products