FDA•MODERATE
Sevillo Fine Foods Slow Roasted Diced Tomatoes
Sevillo Fine Foods is recalling 24 lb bulk boxes of frozen Slow Roasted Diced Tomatoes due to potential metal fragment contamination.
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FDA•MODERATEOxycodone Hydrochloride Tablets, USP 5 mgAmerican Health Packaging is recalling Oxycodone Hydrochloride 5 mg tablets due to defective blister card seals that allow tablets to fall out.
FDA•MODERATEPIE PAK Trolley SystemEdermy is recalling PIE PAK trolley system models P2HC-A, P2HC-S, and P2HC due to a lack of required 510(k) clearance.
2 products
FDA•MODERATESpicy Breakfast BurritoMG Foods is recalling 10 oz Spicy Breakfast Burritos due to potential contamination with small hard plastic fragments.
FDA•LOWSodexo Stars Saccharin Pink PacketsSodexo Stars Saccharin (Pink) packets are recalled due to undeclared aspartame, which may pose a risk to individuals with PKU.
FDA•MODERATEOctopus Nuvo Tissue StabilizerMedtronic is recalling Octopus Nuvo Tissue Stabilizer (TSMICS1) due to incorrect tubing assembly that may affect surgical tissue stabilization.
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•Karison Panjiri, Pinni, and LaddooKarison is recalling Panjiri, pinni, and laddoo products due to undeclared milk, posing a risk to consumers with milk allergies.
FDA•Spring & Mulberry Mint Leaf Chocolate BarSpring & Mulberry is recalling its Mint Leaf Date Sweetened Chocolate Bar due to potential Salmonella contamination.
FDA•Outside the Breadbox Bread CrumbsOutside the Breadbox is recalling Bread Crumbs due to undeclared egg and milk allergens.
FDA•MODERATESonic TotsMcCain Foods is recalling Sonic Tots 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 Replacement PlateauWaldemar Link is recalling the Endo-Model Replacement Plateau due to a risk of longitudinal fracture that may cause bushing detachment.
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•HerbsForever Dietary SupplementsHerbsForever is recalling Gastro Care and Hingwastika dietary supplements due to undeclared wheat, which poses a risk to those with allergies.
FDA•Modern Warrior Dietary Supplement CapsulesModern Warrior is recalling dietary supplement capsules containing undeclared 1,4-DMAA, aniracetam, and tianeptine.
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•Klong Kone Shrimp PasteGusto Group is recalling Klong Kone Shrimp Paste due to potential lead contamination.
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 Dialysis Insertion KitsMedline is recalling dialysis insertion kits due to defective Tego Connector silicone seals that may cause leakage or therapy interruption.
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•Silintan Dietary Supplement Capsules123Herbals is recalling Silintan dietary supplement capsules because they contain undeclared meloxicam.
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 (Model KD-V411M-1520) due to a manufacturing defect that may cause device deformation.
30 products
FDA•MODERATEMedline Surgical Convenience KitsMedline is recalling various surgical convenience kits due to potential issues with sterilization and packaging calibration.
62 products
FDA•MODERATEPhilips Brilliance iCT and Spectral CT 7500 Gantry RotorPhilips is recalling Brilliance iCT and Spectral CT 7500 systems because improperly torqued gantry fasteners may cause rotor parts to detach.
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 record linking.
FDA•MODERATEMedline Convenience KitsMedline is recalling convenience kits due to potential sterility issues caused by equipment calibration errors.
58 products- FDA•MODERATEKarison Panjiri
Karison 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 Supplement
HerbsForever 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•Primavera TamalesPrimavera is recalling its Tamales due to potential Listeria monocytogenes contamination.
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.