FDA•MODERATE
ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich
F&S Fresh Foods recalls ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwiches over undeclared sesame.
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FDA•MODERATEDivided Sunset Multi Collagen PeptidesDivided Sunset Multi Collagen Peptides are recalled for failing to declare egg and fish allergens on the product label.
FDA•MODERATEXanax XR Alprazolam 3 mg TabletsViatris is recalling Xanax XR 3 mg tablets (NDC 58151-506-91) due to failed dissolution specifications.
FDA•MODERATEIsotretinoin Capsules, USP, 40 mgTeva is recalling 40 mg Isotretinoin Capsules due to potency issues.
2 products
NHTSA•MODERATELexus RC, GS, IS Fuel PumpToyota is recalling 2015–2022 Lexus RC, 2016–2020 GS, and 2022 IS vehicles over fuel pump failure risk.
NHTSA•MODERATEForest River Westbrook and Avenger Travel TrailersForest River is recalling 2026 Westbrook and Avenger travel trailers with incorrect dry weight labels that may cause overloading and crash risk.
FDA•MODERATEB.R.A.H.M.S PlGF Plus KRYPTORBrahms recalls PlGF Plus KRYPTOR test (REF 859075N) due to QC underestimation risk causing false preeclampsia risk classification.
FDA•MODERATEVancomycin HCl 1.5g in 250mL Sodium Chloride InjectionFagron recalls Vancomycin HCl 1.5g/250mL injection due to sterility concern.
5 products
FDA•MODERATEGeri-Care Artificial Tears Lubricant Eye DropsGeri-Care Artificial Tears Lubricant Eye Drops (0.5 oz, NDC 68788-7266-0) recalled due to lack of sterility assurance.
FDA•CRITICALMedline Convenience Kits with Namic RA SyringesMedline recalls convenience kits with Namic RA syringes over risk of loose connection or disconnection during use.
25 products
FDA•MODERATEARTIS pheno and ARTIS Icono Biplane X-ray SystemSiemens is recalling ARTIS pheno and ARTIS Icono X-ray systems (Models 10849000, 11327600, 11328100, 11327700) due to erroneous dose display during patient exams.
FDA•MODERATESpacelabs Multi-parameter Command Module Model 91496Spacelabs is recalling Model 91496 Multi-parameter Command Module due to circuit board issue causing inaccurate cardiac output readings.
NHTSA•MODERATECan-Am Origin Electric Motorcycle Front Brake CaliperBRP is recalling 2025 Can-Am Origin electric motorcycles for front brake caliper failure risk.
FDA•MODERATELIQUID BLENZ: 13 productsLiquid Blenz recalls 13 herbal tonics and bitters over under-processing, risking botulism.
13 products
FDA•MODERATECook Arterial Pressure Monitoring TrayCook recalls Arterial Pressure Monitoring Trays due to incorrect expiration dates.
19 products
FDA•MODERATESee Luer Cap Set MPC-130Molded Products is recalling See Luer Cap Set MPC-130 due to threaded sleeve detachment risk.
NHTSA•MODERATEGreenpower Nano Beast and Beast School Bus Cross View MirrorGreenpower is recalling 2020–2024 Nano Beast and 2021–2024 Beast school buses with missing Cross View Mirror warning labels, risking driver misuse and crashes.
NHTSA•MODERATEPierce Arrow XT/Enforcer/Impel/Velocity Firm-On-Ground LightPierce is recalling 2015–2026 Arrow XT/Enforcer/Impel/Velocity aerial firetrucks; firm-on-ground light may fail to deactivate when stabilizer loses ground contact.
NHTSA•MODERATEHyundai Ioniq 6, Genesis G90, Santa Fe Seat Belt AnchorsHyundai is recalling Ioniq 6, Genesis G90, and Santa Fe vehicles over detachable seat belt anchors that may fail to restrain occupants.
FDA•CRITICALWawa Beverage: 4 productsWawa recalls 16 oz Iced Tea Lemon, Diet Iced Tea Lemon, Diet Lemonade, and Fruit Punch over undeclared milk allergen.
4 products
FDA•MODERATEZarlengo Italian Ice: 5 White Round Food And Freezer GradesZarlengo's recalls Chocolate Gelato (multiple sizes) over undeclared soy allergen.
5 products
FDA•MODERATEFresenius Kabi: Multiple Sale NDC Number InjectionsFresenius Kabi recalls 14 lots of Sodium Chloride and Dextrose Injections due to sterility concerns.
14 products
FDA•MODERATEXTANT MEDICAL Xpress Pedicle Screw SystemXTANT MEDICAL is recalling Xpress Pedicle Screw System 6.5 x 50 mm (X073-6555-DL) due to mislabeling identifying incorrect screw length.
FDA•MODERATETornier HRS Max Tuberosity Body and Trial PartsTornier is recalling shoulder system components incorrectly labeled as HRS Max parts, as they are incompatible with the HRS Max system.
NHTSA•MODERATEMercedes-Benz Drive Shaft Universal JointMercedes-Benz is recalling certain 2018–2020 E-Class and Maybach models due to drive shaft universal joint breakage risk.
NHTSA•MODERATEAutocar ACX Xpeditor Winter Front CoverAutocar recalls 2025–2026 ACX Xpeditor vehicles; winter front cover may disable forward collision warning system.
NHTSA•MODERATEGraco SnugRide Turn & Slide Infant Car SeatGraco SnugRide Turn & Slide infant car seats may detach from the base in a crash, posing injury risk.
3 products
NHTSA•CRITICALIS300 Slave Cylinder Conversion Kit Adapter PlateSleepy Customs is recalling IS300 Slave Cylinder Conversion Kits; adapter plate may separate, causing loss of clutch and gear-shift function.
FDA•MODERATESmart & Simple Turmeric PelletsSmartPak Equine is recalling Smart & Simple Turmeric Pellets for horses due to elevated aflatoxin levels.
FDA•CRITICALRaw Farm: 5 productsRaw Farm recalls raw cheddar cheeses over possible E. coli O157:H7 outbreak.
5 products
FDA•MODERATECoconut Drink 1HEYTEA USA INC is recalling Coconut Drink 1 (1L, UPC 673367992785) due to undeclared milk.
FDA•MODERATEMedline Anterior Hip Pack Biopsy ValveMedline is recalling Anterior Hip Packs containing Olympus biopsy valves over risk of rubber fragment detachment.
8 products
FDA•MODERATESIGNA Premier MR Scanner Magnet FittingsGE Healthcare is recalling SIGNA Premier MR scanners due to ferrous magnet fittings that could cause personnel injury during service.
FDA•MODERATEMedtronic MiniMed Insulin PumpsMedtronic MiniMed recalls all Paradigm, 600, and BLE 700 series insulin pumps over insulin delivery errors that can cause severe hypoglycemia or ketoacidosis.
14 products
FDA•MODERATEBurlington Medical Wrap ApronsBurlington Medical wrap aprons may lose shielding effectiveness over time.
13 products
FDA•MODERATEOXOID Microbact 12L Listeria Identification KitOxoid is recalling Microbact 12L Listeria Kit (MB1128A, Lot 4494873) due to risk of incorrect organism identification from ambiguous color reactions.
- Device RecallFDA•CRITICALPhilips Respironics Trilogy Evo O2 Ventilator
Philips Respironics recalls Trilogy Evo O2 ventilators (SW 1.05.15.00) over delayed obstruction alarm.
4 products 
FDA•MODERATECardinal Health Monoject Tuberculin Syringe 1 mLCardinal Health is recalling Monoject Tuberculin Syringes (Catalog 1180100777) that contain U-100 insulin syringes instead, risking dosing errors.
NHTSA•MODERATEBMW K 1600 and Grand America Reverse Gear Control UnitBMW is recalling 2017–2025 K 1600 GT/GTL/B and 2018–2025 Grand America motorcycles over reverse gear control unit overheating and fire risk.
NHTSA•MODERATEChevrolet Malibu Rearview CameraGM recalls 2023–2025 Chevrolet Malibu rearview cameras that may display distorted or blank images.
NHTSA•MODERATEChevrolet Corvette Rear Turn Signal Warning SystemGM is recalling 2025–2026 Chevrolet Corvette models over a software error that may prevent detection of rear turn signal failure.
NHTSA•MODERATEKeystone Montana Fifth Wheel UnderbellyKeystone is recalling 2026 Montana fifth wheel trailers; underbelly may detach during transit, creating road hazard.
FDA•CRITICALDouble Down Deer FeedProducers Cooperative Association is recalling Double Down deer feed products due to elevated aflatoxin levels.
2 products
FDA•MODERATEPurina Nature's Match Sow & Pig Complete FeedPurina is recalling 50 lb bags of Nature's Match Sow & Pig Complete Feed (UPC 804273051451) due to elevated Deoxynivalenol levels.
FDA•LOWTops Markets: 2 Peeled GarlicsPeeled Garlic recalled over Clostridium botulinum risk from temperature abuse.
2 products
FDA•MODERATELucerne 2% Cottage Cheese 24 ozLucerne 2% Cottage Cheese 24 oz recalled over possible metal fragments.
FDA•LOWSuper World Trading: 3 Heshan Mei Heong Yuen Food Pte NiesMei Heong Yuen roasted peanuts recalled over banned cyclamate sweetener.
3 products
FDA•MODERATEMeclizine Hydrochloride Tablets 12.5 mgAmerican Health Packaging is recalling Meclizine Hydrochloride 12.5 mg tablets (NDC 60687-775-65 and 60687-775-11) due to failed tablet specifications.
FDA•MODERATEeTRAX Needle System Starter Kit 12GCivco recalls eTRAX Needle System Starter Kit 12G (Part 667-149) due to sensor programming error causing incorrect needle tip position.
8 products
FDA•CRITICALCentrosFLO Hemodialysis CathetersMerit Medical recalls CentrosFLO Hemodialysis Catheters over sheath introducer defect that may cause hemorrhage and other serious complications.
5 products