FDA•MODERATE
AQ 120 GFEW Aquarion Preserved Cartridges
Encon Safety Products is recalling AQ 120 GFEW Aquarion Preserved Cartridges due to cGMP manufacturing deviations.
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FDA•MODERATEVITEK 2 Gram-negative Susceptibility CardsBioMérieux is recalling 30+ VITEK 2 susceptibility card variants over risks of quality control failures and false resistant test results.
2 products
FDA•MODERATERaz Mobile Shower Commode ChairsRaz Design is recalling various mobile shower commode chairs due to a seat bracket installation issue that may cause seat instability.
2 products
FDA•MODERATEMedline Nail KitMedline is recalling the Nail Kit (Model DYKM1528) due to a potential sterility assurance issue with the included wound wash.
5 products
FDA•MODERATEEMPOWR Acetabular System and Knee Tibial InsertsEncore Medical is recalling EMPOWR acetabular liners and knee inserts due to a packaging discrepancy that may cause surgical delays.
2 products
FDA•MODERATEHalyard Transport Bag Kit LIFE0080-01Halyard Transport Bag Kit LIFE0080-01 recalled due to Tyvek bag seal issue that may compromise sterility.
FDA•MODERATEATEC Lateral Navigation Disc Prep InstrumentsAlphatec Spine is recalling ATEC Lateral Navigation Disc Prep Instruments due to a design issue with the navigated array connection geometry.
2 products
FDA•MODERATELanreotide Injection 120 mg/0.5 mLCipla is recalling Lanreotide Injection 120 mg/0.5 mL (NDC 69097-870-67) due to particulate matter contamination.