FDA•MODERATE
Fluocinonide 0.05% Cream
Taro Pharmaceuticals is recalling Fluocinonide 0.05% Cream due to out-of-specification viscosity results.
3 productsFilters
Category
Agency
Severity
All Recalls
Back to home ←
FDA•LOWFarmina Pet Foods N&D Tropical Selection Dog FoodFarmina Pet Foods N&D Tropical Selection dog food (22 lb, UPC 8 01027 60423 85) recalled due to mislabeling—front lists salmon, back lists lamb.
FDA•MODERATEOxoid Salmonella 9-O Agglutinating SeraRemel Europe is recalling Oxoid Salmonella 9-O Agglutinating Sera due to potential cross-reactivity and misidentification of serotypes.
FDA•MODERATEAvitene Ultrafoam Microfibrillar Collagen HemostatDavol is recalling Avitene Ultrafoam Microfibrillar Collagen Hemostat (Catalog 1050030) due to potential inspect fragment contamination.
FDA•MODERATEOlympus OER-ELITE Endoscope Reprocessor Connecting TubesOlympus is recalling OER-ELITE Endoscope Reprocessor Connecting Tubes (model MAJ-2110) due to a risk of premature lock lever failure.
12 products
FDA•LOWHeraeus PALAMIX uno Mixing SystemHeraeus is reducing the shelf life of the PALAMIX uno mixing system to 17 months due to a potential mixing rod detachment risk.
2 products
FDA•CRITICALVOCSN V+Pro Respiratory SystemVentec is recalling VOCSN V+Pro respiratory systems (REF: PRT-01198-000, PRT-01185-000) due to potential oxygen leaks that may increase fire risk.
FDA•MODERATEDEX Ophthalmic Tissue ForcepsKatalyst Surgical is updating the Instructions for Use for DEX Ophthalmic Tissue Forceps and 23ga DEX NanoTapered AWH Forceps.
12 products
FDA•MODERATEBioCera Fibers Bone Void FillerOrthorebirth is recalling BioCera Fibers bone void filler products that fall outside of standard manufacturing specifications.
2 products
FDA•CRITICALOmnicell i.v.STATION Syringe Label StockOmnicell is recalling i.v.STATION syringe label stock due to a risk of mislabeled syringes during IV medication compounding.
FDA•MODERATEOmnipaque (iohexol) InjectionGE Healthcare is recalling Omnipaque (iohexol) injection due to the presence of particulate matter.
2 products
NHTSA•MODERATENova Bus LFS Transit Bus Seat BeltNova Bus is recalling LFS and LFS Artic transit buses (2016–2023) due to driver seat belt tension-relieving device failure.
NHTSA•MODERATEToyota and Lexus Load Carrying Capacity LabelToyota and Lexus are recalling 2024–2026 Tundra, Tacoma, RAV4, and other models with incorrect load capacity labels that may cause overloading and crash risk.
NHTSA•MODERATELexus LX Front Passenger Air Bag SystemToyota is recalling 2022–2024 Lexus LX vehicles over front passenger air bag deployment risk from seat-frame clearance issues.
NHTSA•MODERATEStoryteller GXV Hilt Entry StepsStoryteller is recalling 2024–2026 GXV Hilt RVs; entry steps may deploy while in transit, increasing crash risk.
NHTSA•MODERATEBentley Bentayga Tire PlacardBentley is recalling 2025 Bentayga vehicles with incorrect tire placard information that may lead to wrong tire size or pressure.
FDA•MODERATEMemantine Hydrochloride Extended-Release 7 mg CapsulesMajor Pharmaceuticals is recalling Memantine Hydrochloride Extended-Release 7 mg capsules (NDC 0904-6734-61) due to failed dissolution specifications.
FDA•CRITICALSalute Seasonings Ground All SpiceSalute Seasonings Ground All Spice (16 oz) recalled for possible Salmonella contamination.
FDA•CRITICALAyco Fresh CantaloupeAyco Farms is recalling whole fresh cantaloupes due to potential Salmonella contamination.
FDA•MODERATEHamilton AutoLys STAR Protocol Configuration Tool SoftwareFoundation Medicine recalls PCT software v1.3.0 for Hamilton AutoLys STAR due to risk of spontaneous software closures during protocol execution.
FDA•MODERATERemel Yeastone BrothRemel is recalling Yeastone Broth due to the potential for incorrect antimicrobial susceptibility testing results during quality control.
FDA•LOWGarland Fresh Peeled GarlicGarland Fresh Peeled Garlic 6 oz. bags are recalled due to potential Clostridium botulinum contamination from temperature abuse.
2 products
FDA•LOWSunRidge Farms Organic Black BeansSunRidge Farms Organic Black Beans are recalled due to potential contamination with haloxyfop and thiamethoxam pesticides.
3 products
FDA•CRITICALNamic Angiographic ManifoldMedline is recalling Namic Angiographic Manifolds due to the presence of particulate matter within the fluid path.
14 products
FDA•MODERATEICU Medical Oncology Extension SetICU Medical is recalling Oncology Extension Set REF: CL3960 due to a potential leak that could cause therapy interruption or hazardous exposure.
NHTSA•MODERATEWinnebago Motorhome Front Turn SignalsWinnebago is recalling 2017–2022 Brave, Itasca Sunova, Adventurer, and Sunstar motorhomes over undersized front turn signal lenses.
NHTSA•MODERATESetra S417 and S407 Dashboard Switch IlluminationDaimler Coaches is recalling 2009–2020 Setra S417 and 2012–2019 S407 buses due to dashboard switch illumination failures that may distract drivers.
NHTSA•MODERATEHino 2026 Commercial Vehicles U-Bolt InstructionsHino is recalling 2026 NV7G, NV7D, NJ7E, NJ7D, NH7K, NE7D, and NH7G vehicles over incorrect U-bolt maintenance instructions that may cause bolt breakage and crash risk.
FDA•MODERATEBooey's Dragon's Breath SauceBooey's Dragon's Breath sauce is recalled for undeclared fish (anchovy) and sesame allergens.
FDA•MODERATEGentuity HF-OCT Imaging SystemGentuity is correcting software versions 21.11–23.3.13 for the HF-OCT Imaging System to prevent inaccurate longitudinal measurements.
FDA•MODERATEOlympus Thunderbeat II ShearsOlympus is recalling Thunderbeat II Shears (Model TB2-0520FC) due to the risk of a distal tip component detaching during use.
4 products- Device RecallFDA•MODERATEGenius Digital Diagnostics System Review Station Display
Hologic is correcting Genius Review Station displays (Model CMP-01669) due to unauthorized user modifications to validated monitor settings.
FDA•MODERATEHiResolution Bionic Ear System M Zn-Air Battery PakAdvanced Bionics is recalling M Zn-Air Battery Paks for sound processors due to a non-compliant battery door that lacks tool-based access.
2 products
FDA•MODERATETangent Single Use Digital CatheterTangent Endoscopy is recalling single-use digital catheters due to potential fractures at the distal shaft tip.
FDA•MODERATEVancomycin HCl InjectionFagron is recalling Vancomycin HCl injection due to sterility concerns and a potential detachment of the administration port's break-off part.
5 products
NHTSA•MODERATEMercedes-Benz GLC Center Rear Seat BeltMercedes-Benz is recalling 2026 GLC models with center rear seat belts that may fail to properly restrain child seats.
NHTSA•MODERATEHyundai Palisade Seat Belt Status IndicatorHyundai is recalling 2026 Palisade and Palisade Hybrid (Limited/Calligraphy trims) over faulty third-row seat belt status indicator that may fail to alert unfastened occupants.
NHTSA•MODERATEAltec AC Series Crane and DT Series Digger Derrick Chassis Lighting HarnessAltec is recalling 2025 AC Series Crane and DT Series Digger Derrick vehicles due to missing chassis lighting harness that may disable body or trailer lights.
NHTSA•MODERATEGrand Design Lineage Motorhome Entry StepsGrand Design is recalling 2025–2026 Lineage motorhomes; entry steps may deploy while in transit, increasing crash risk.
NHTSA•MODERATERam ProMaster Emergency Exit WindowBraun is recalling 2023–2024 Ram ProMaster vehicles with incorrect emergency exit window glass that fails FMVSS 226 safety standards.
NHTSA•MODERATEKia Telluride Hybrid Second-Row Power SeatKia is recalling 2027 Telluride Hybrid second-row power seats that may fail to detect and stop for a person.
FDA•MODERATEExchange Select Honey Lemon Cough DropsExchange Select Honey Lemon Cough Drops are being recalled due to manufacturing facility observations that may impact product quality.
15 products
FDA•MODERATEFurosemide Tablets, USP 80 mgLeading Pharma is recalling Furosemide Tablets 80 mg (NDC 69315-118-01) due to N-nitroso-Furosemide above recommended limits.
FDA•MODERATEFoundationOne CDx Sequencing Agent SEQ0067Foundation Medicine is recalling Sequencing Agent SEQ0067 component of FoundationOne CDx due to possible false-positive BARD1 variants.
FDA•LOWBee Well Wildflower HoneyBee Well is recalling three sizes of Wildflower Honey because testing indicated high C4 sugar content, meaning it is not 100% pure honey.
FDA•MODERATEProdisc C SK U.S. Cervical Disc ImplantCentinel Spine is recalling Prodisc C SK U.S. cervical disc implants due to a labeling mix-up involving 5mm and 6mm height specifications.
2 products
CPSC•Frigidaire Gas RangesFrigidaire is recalling 23 gas range models (serials VF52200000–VF54399999) due to delayed oven ignition posing a burn hazard.
CPSC•Amazon Basics Camping Folding Pocket KnifeAmazon Basics Camping Folding Pocket Knife (model B0DM5BJK3H) recalled due to blade mechanism failure and laceration hazard.
CPSC•Tainoki Fine Furniture Office ChairsTainoki is recalling office chairs (models M7016O, M7004O, M7074O) with bases that can bend, creating a fall hazard.
CPSC•Goregent Infant WalkerGoregent infant walkers (Model 901) sold on Amazon violate safety standards and pose fall hazards.