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 potential sterility issues with the included saline wound wash.
5 products
FDA•MODERATEEMPOWR Acetabular System and Knee Tibial InsertsEncore Medical is recalling EMPOWR acetabular system liners and knee tibial inserts due to a packaging discrepancy that may delay surgery.
2 products
NHTSA•MODERATELS2 Rebellion Motorcycle HelmetLS2 Rebellion helmets (XL, XXL, July 2024–July 2025) recalled for inadequate impact protection.
NHTSA•MODERATERivian R1S and R1T Toe Link JointRivian is recalling 2022–2025 R1S and R1T vehicles; toe link joint may separate after service, increasing crash risk.
NHTSA•MODERATEBlue Bird All American Transit Bus 12-Volt CableBlue Bird is recalling 2022–2024 All American transit buses over a loose 12-volt cable that may cause loss of brake assist, drive power, and steering.
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.