FDA•MODERATE
Adndale Magnesium Glycinate Gummies
Adndale Magnesium Glycinate Gummies are being recalled due to the presence of undeclared melatonin.
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FDA•MODERATEBD Connecta Luer-Lok StopcockBD is recalling Connecta Luer-Lok stopcocks due to a potential connection failure at Port C when using plastic luer-lok syringes.
FDA•MODERATESplashwire Hydrophilic Guide WireMerit Medical is recalling various Splashwire Hydrophilic Guide Wire models due to unsealed pouches that may compromise device sterility.
2 products
NHTSA•MODERATEPiaggio Liberty 50 and 150 MotorcyclesPiaggio is recalling 2026 Liberty 50 and 150 motorcycles due to an electrical fault that may cause the headlights to unexpectedly turn off.
NHTSA•MODERATEToyota BZ, Lexus RZ, and Subaru Solterra Electric VehiclesToyota is recalling 2026 Toyota BZ, Lexus RZ, and Subaru Solterra EVs due to an ECU fault that may cause a loss of drive power.
NHTSA•MODERATEFarber Specialty Emergency Vehicles Touch ScreenFarber Specialty is recalling 2025-2026 emergency vehicles because the touchscreen may fail, disabling emergency lights and equipment.
NHTSA•MODERATECadillac Vistiq Third-Row Power SeatbackGM is recalling 2026-2027 Cadillac Vistiq vehicles because the third-row power seatback may fail to reverse, posing an entrapment risk.
FDA•MODERATEBuprenorphine HCl InjectionPar Health is recalling Buprenorphine HCl Injection due to crystallization identified as Buprenorphine free base.
FDA•MODERATETriathlon Universal Baseplate Size 3/4Stryker recalls Triathlon Universal Baseplates due to size mislabeling in packaging.
2 products
FDA•MODERATEMedline Red Rubber Latex Urethral CathetersMedline recalls Red Rubber Latex Urethral Catheters (REF DYND13508–DYND13522, DYND13614/16) over surface, connector, and diameter defects.
34 products
FDA•MODERATEGiraffe OmniBed Canopy SoffitGE HealthCare recalls Giraffe OmniBed incubator/warmer over canopy soffit fastener risk that could injure patients.
3 products
FDA•MODERATEConMed AirSeal 5 mm Access PortConMed recalls AirSeal 5 mm Access Port (iASB5-150) over overpressure alert risk.
11 products- Device RecallFDA•MODERATESTAAR ICL Calculation Software
Staar Surgical is recalling Version 8.00 of its ICL Calculation Software due to a coding error affecting toric lens orientation diagrams.
2 products 
FDA•MODERATEPhilips MultiDiagnost Eleva Hand SwitchPhilips recalls MultiDiagnost Eleva systems over hand switch that may not release, risking unintended radiation.
3 products
FDA•MODERATENutrisystem Chocolate CheesecakeNutrisystem is recalling Chocolate Cheesecake 2 oz packages due to an undeclared soy allergen.
FDA•MODERATEGreat Value Hawaiian Roll 4pkGreat Value Hawaiian Roll 4pk recalled over oily substance on food-contact packaging; product never reached store shelves.
FDA•MODERATERitmed Neurological SpongesAMD Medicom recalls Ritmed Neurological Sponges due to elevated endotoxin risk; full REF list on FDA page.
2 products
FDA•MODERATEdirectCHECK ACT-LR Whole Blood Quality ControlAccriva Diagnostics is recalling directCHECK ACT-LR whole blood quality control, level 2, due to incorrect performance range labeling.
FDA•MODERATEMID DOLCIARIA SRL: 2 Via Casalini BelpassosMID DOLCIARIA recalls Cannoli Siciliani and Crunchy Cannoli Gluten Free over unapproved colors E140/E141.
2 products
FDA•MODERATETrigen Proximal Straight Humeral NailSmith & Nephew is recalling the Trigen Proximal Straight Humeral Nail due to a manufacturing error that may cause surgical delays or revision.
NHTSA•MODERATEStoryteller GXV Hilt Alternator PulleyStoryteller is recalling 2024-2026 GXV Hilt vehicles due to an alternator pulley failure that may cause a loss of power brakes and steering.
FDA•MODERATEAripiprazole 30 mg TabletsAjanta Pharma is recalling Aripiprazole 30 mg tablets due to a mix-up with Voriconazole 50 mg tablets.
FDA•MODERATEMedtronic O-arm O2 Imaging SystemMedtronic is recalling the O-arm O2 Imaging System due to a firmware anomaly that may cause image artifacts during clinical use.
FDA•MODERATEHarmonyAIR A-Series Surgical Lighting SystemHarmonyAIR A-Series surgical lights recalled: intensity buttons may detach.
2 products
FDA•MODERATEHarmonyAIR A-Series Surgical Lighting SystemSteris is recalling HarmonyAIR A-Series Surgical Lighting Systems due to a risk of paint delamination on the light heads.
NHTSA•MODERATEForest River XLR Toy Hauler Recreational TrailersForest River is recalling 2023-2024 XLR Toy Hauler trailers due to an incorrect GVWR that may lead to vehicle overloading and crash risk.
NHTSA•MODERATEWabash 2027 Van Trailer Rear Impact GuardWabash is recalling 2027 van trailers due to improperly tightened rear impact guard bolts that may fail to meet federal safety standards.
- Equipment RecallNHTSA•MODERATEWaymo 5th Generation Automated Driving Systems
Waymo is recalling 5th Generation ADS software that may allow vehicles to enter and drive through closed freeway construction zones.
FDA•MODERATEPepperoni Rolls 5 ozPepperoni Rolls recalled for undeclared milk allergen and improper refrigeration; 5 oz packages.
FDA•MODERATEDabur India: Multiple Made In India ProductsDabur India recalls 14 OTC topical products over CGMP deviations.
14 products
FDA•MODERATEChlorthalidone 25 mg TabletsChlorthalidone 25 mg tablets are being recalled due to failed dissolution specifications.
FDA•MODERATEAlyacen 7/7/7 TabletsGlenmark is recalling Alyacen 7/7/7 tablets due to out-of-specification results for total impurities.
FDA•MODERATEVasopressin 2 Units/2 mL SyringesIntegraDose is recalling Vasopressin 2 Units/2 mL syringes due to subpotency, which may cause the drug to be ineffective.
FDA•MODERATEPAI: Multiple Kerr Insta-char In An ProductsVistaPharm recalls Kerr Insta-Char activated charcoal (25g/50g) for failing OTC monograph requirements.
4 products
FDA•MODERATEMedline EBSI KitMedline recalls EBSI Kit (EBSI1534) due to cracked butyrate tubing and recalled MASTISOL adhesive.
42 products
NHTSA•MODERATEWinnebago Revel and Revel Sport Recreational VehiclesWinnebago is recalling 2026-2027 Revel and Revel Sport RVs due to incorrect tire information labels that may lead to improper tire installation.
NHTSA•MODERATEThomas Built SAF-T-LINER HDX2 School Bus Body JointsDaimler is recalling 2027 Thomas Built SAF-T-LINER HDX2 school buses due to insufficient body joint strength that may increase injury risk.
NHTSA•MODERATEKawasaki W230 Motorcycle Turn Signal BulbsKawasaki is recalling 2025-2026 W230 motorcycles due to defective turn signal bulbs that may fail and increase the risk of a crash.
NHTSA•MODERATEAltec AT Series Aerial DeviceAltec is recalling 2014-2026 AT Series Aerial Devices because a missing transmission park interlock may cause unexpected vehicle movement.
NHTSA•MODERATEWaltco MDV Series Liftgate Deck PinsMarion Body Works is recalling Waltco MDV series liftgates on Morgan dry vans because broken deck pins may cause the platform to fall.
NHTSA•MODERATELand Rover Defender, Discovery, and Range Rover Air BagLand Rover is recalling various 2020-2026 Defender, Discovery, and Range Rover vehicles due to an air bag clockspring corrosion risk.
FDA•MODERATENiacin Extended-Release Tablets 1,000 mgGolden State Medical Supply is recalling Niacin Extended-Release Tablets, 1,000 mg, due to failure to meet dissolution specifications.
2 products
FDA•MODERATEFresh Roast Systems ColorTrack InstrumentFresh Roast Systems is recalling the ColorTrack instrument (Model BENCH R-100) due to a potential laser safety hazard.
FDA•MODERATEHalyard Pain PackAVID Medical recalls Halyard Pain Pack kits (AMPK48-01) over possible lack of sterilization.
4 products
FDA•MODERATEMOSAIQ Oncology Information SystemElekta is recalling the MOSAIQ Oncology Information System due to a software error that may prevent the loading of baseline shift plans.
FDA•MODERATEBoston Scientific Orca Air/Water and Suction ValvesBoston Scientific is recalling Orca single-use air/water and suction valves due to reports of the suction button sticking during use.
- Device RecallFDA•MODERATEMerlin Patient Care System Programmer Software
Abbott Medical is recalling Merlin PCS software for the Model 3330 programmer due to a potential failure to terminate pacing tests.
FDA•MODERATEBoston Scientific Clik X AnchorBoston Scientific is recalling the Clik X Anchor due to a potential lack of sterility assurance.
FDA•MODERATEBoston Scientific CSK ElectrodesBoston Scientific recalls CSK reusable electrodes over performance concerns.
4 products
FDA•MODERATEBicarby DialysateFresenius Medical Care is recalling Bicarby Dialysate due to a GTIN labeling error that may result in the use of an incorrect potassium solution.