FDA•MODERATE
Octopus Nuvo Tissue Stabilizer
Medtronic is recalling Octopus Nuvo Tissue Stabilizer (TSMICS1) due to incorrect tubing assembly that may affect surgical tissue stabilization.
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FDA•MODERATELaerdal Compact Suction Unit 4 RTCALaerdal is recalling Compact Suction Unit 4 RTCA models due to potential electromagnetic noise interference exceeding safety standards.
FDA•MODERATESpectrum IQ Infusion PumpBaxter is recalling Spectrum IQ Infusion Pumps (Model 3570009) because they were released without full occlusion alarm testing.
FDA•MODERATESonic Tots Frozen PotatoesMcCain Foods is recalling Sonic Tots frozen potato products due to potential contamination with small hard plastic fragments.
2 products
FDA•MODERATEIsotretinoin 40 mg CapsulesTeva is recalling Isotretinoin 40 mg capsules due to superpotency and subpotency concerns that may affect treatment efficacy or safety.
2 products
FDA•MODERATEEndo-Model Knee Implant PlateauWaldemar Link is recalling the Endo-Model Replacement Plateau due to a risk of fracture that may cause the bushing to detach.
13 products
FDA•CRITICALADM Animal Nutrition MasterPlex 75P 30/30 RU 55010CDHADM Animal Nutrition recalls MasterPlex 75P 30/30 RU 55010CDH medicated cattle feed due to incorrect labeling causing monensin/urea toxicity.
FDA•MODERATEFurosemide Tablets USP 40 mgRising Pharmaceuticals is recalling Furosemide Tablets 40 mg (NDC 64980-563-10) due to foreign substance contamination.
FDA•MODERATESea Moss Gel SuperfoodDiva Fam is recalling Sea Moss Gel Superfood due to potential Clostridium botulinum contamination.
14 products
FDA•MODERATEAPTUS 2.5 TriLock Screw 16mmMedartis is recalling APTUS 2.5 TriLock Screw 16mm (Model A-5750.16/1) due to a packaging mix-up with 2.8mm screws.
2 products
FDA•MODERATEMaquet Venous Bubble SensorMaquet is recalling Venous Bubble Sensors for 3/8" x 3/32" tubing due to cable durability issues that may cause sensor failure.
FDA•MODERATEFDR Visionary Suite X-ray GeneratorFDR Visionary Suite X-ray generators are being recalled due to a risk of overheating and smoke caused by faulty electromagnetic contactors.
FDA•MODERATEDiowave 250W Laser SystemDiowave 250W Laser System recalled; software update needed to correct power output exceeding FDA-cleared 60W limit.
FDA•CRITICALOutside The Breadbox Bread CrumbsOutside The Breadbox is recalling 8 oz Bread Crumbs due to undeclared egg and milk allergens.
FDA•MODERATESmoked Grouper DipIsland Crab Corporation is recalling Smoked Grouper Dip due to undeclared milk, eggs, and sodium metabisulfite.
FDA•MODERATEMedline Kits with Tego ConnectorsMedline is recalling kits with Tego Connectors due to seal defects that may cause fluid leakage, therapy delays, or contamination risks.
6 products
FDA•MODERATEOlympus ShockPulse-SE Lithotripsy System GeneratorOlympus is recalling ShockPulse-SE Lithotripsy System generators due to a mis-wired component that may cause treatment delays.
2 products
FDA•MODERATEGluten Free Seasoned Vegan Pizza CrustRich Products Corp is recalling Gluten Free 14" Seasoned Vegan Pizza Crust due to undeclared milk and egg allergens.
2 products
FDA•MODERATEHannaford Hamburger Dill Pickle ChipsHannaford hamburger dill pickle chips (UPC 0 41268 14889 9) recalled due to glass contamination.
FDA•MODERATEOlympus Single Use 3-Lumen Sphincterotome VOlympus is recalling the Single Use 3-Lumen Sphincterotome V due to a manufacturing defect that may cause the device to deform and lose function.
30 products
FDA•MODERATEMedline Convenience KitsMedline is recalling various surgical and biopsy convenience kits due to potential issues with sterilization and packaging equipment calibration.
62 products
FDA•MODERATEPhilips Brilliance iCT Gantry Rotor FastenersPhilips is recalling Brilliance iCT CT systems because loose gantry rotor fasteners could cause parts to become unsecured or expelled.
4 products- 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 linking.
FDA•MODERATEMedline Convenience KitsMedline is recalling convenience kits due to potential issues with the sterilization process that may affect product sterility.
58 products
FDA•MODERATEKarison PanjiriKarison is recalling Panjiri due to an undeclared milk 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 dislodgement of the deaeration chamber 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•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 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
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.