FDA•MODERATE
Philips Brilliance iCT and Spectral CT 7500 Gantry Rotor
Philips is recalling Brilliance iCT and Spectral CT 7500 systems because improperly torqued gantry fasteners may cause rotor parts to detach.
4 productsMedical Devices Recalls
LatestAll recalls →
- Device RecallFDA•MODERATEMint Lesion Software
Mint Medical is recalling Mint Lesion software versions 3.4.0–3.9.5 due to a risk of data loss or incorrect patient record linking.
FDA•MODERATEMedline Convenience KitsMedline is recalling convenience kits due to potential sterilization issues that may affect product sterility.
58 products
FDA•MODERATEPrismaflex M100 SetVantive is recalling the Prismaflex M100 Set due to a potential deaeration chamber dislodgement from the control unit.
8 products
FDA•LOWStraumann WB Impression Post Closed TrayStraumann is recalling WB Impression Post Closed Tray kits (L 13mm) due to incorrect magenta impression caps instead of brown.
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 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 liners and knee inserts due to packaging errors 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 defect in the navigated array connection geometry.
2 products- Device RecallFDA•FreeStyle Libre 3 and 3 Plus Glucose Sensors
Abbott is recalling FreeStyle Libre 3 and 3 Plus glucose sensors due to the risk of providing incorrect low glucose readings.