Device Recall
FDA•MODERATE
Mint 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.
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FDA•MODERATEMedline Convenience KitsMedline is recalling convenience kits due to potential sterility issues caused by equipment calibration errors.
58 products
FDA•MODERATEKarison PanjiriKarison is recalling Panjiri in 12 oz containers due to undeclared milk, a known allergen.
5 products
FDA•CRITICALCarrot Top Kitchens Lime Ginger HummusCarrot Top Kitchens is recalling 8 oz Lime Ginger Hummus due to undeclared sesame.
5 products
FDA•MODERATEPrismaflex M100 SetVantive is recalling the Prismaflex M100 Set due to a potential deaeration chamber dislodgement risk.
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•CRITICALHerbsForever Gastro Care Herbal SupplementHerbsForever is recalling Gastro Care herbal supplement capsules due to undeclared wheat.
2 products
FDA•MODERATEAQ 120 GFEW Aquarion Preserved CartridgesEncon Safety Products is recalling AQ 120 GFEW Aquarion Preserved Cartridges due to cGMP manufacturing deviations.
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.