NHTSA•MODERATE
Lucid Gravity Seat Belt Anchor Bracket
Lucid is recalling 2025–2026 Gravity vehicles for defective second-row seat belt anchor brackets that may fail in a crash.
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FDA•MODERATEEinstein Bros Bagels Honey Almond ShmearEinstein Bros Bagels is recalling Honey Almond Shmear mislabeled as Plain Cream Cheese due to an undeclared almond allergen.
FDA•MODERATEPantoprazole Sodium Delayed-Release Tablets 40 mgCamber Pharmaceuticals is recalling Pantoprazole Sodium 40 mg tablets (NDC 31722-713-10) due to discoloration.
FDA•MODERATEImmy Myco DDR Trident Neutralization Buffer BImmuno-Mycologics is recalling Myco DDR Trident Neutralization Buffer B due to potential contamination.
FDA•MODERATESpacelabs Ultraview SL Command ModuleSpacelabs is recalling the SL Command Module due to a manufacturing issue with the electrical leakage tester.
2 products
FDA•MODERATEGE Revolution CT SystemsGE is recalling Revolution CT systems due to a security vulnerability in the AW Server software used with the CT Smart Subscription feature.
7 products
FDA•MODERATEAlain Milliat Orange MarmaladeAlain Milliat Orange Marmalade is being recalled due to the potential presence of glass fragments in the product.
FDA•MODERATECrab CakesConnecticut Crab Company is recalling crab cakes sold to food service due to potential Clostridium botulinum contamination.
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.
NHTSA•MODERATEVolvo VNL Brake Release DelayVolvo is recalling 2025–2026 VNL (4) trucks over delayed brake release that increases crash risk.
- NHTSA•MODERATEVolvo Trucks VNL Instrument Panel Display
Volvo Trucks is recalling 2025–2026 VNL (4) vehicles for instrument panel display failure that may hide speedometer and warning lights.
NHTSA•MODERATEVolkswagen Jetta and Taos Instrument PanelVolkswagen is recalling 2025 Jetta and Taos vehicles with instrument panels that may fail to display warning lights or gauges.
NHTSA•MODERATEAston Martin DBX Tire Pressure Monitoring SystemAston Martin is recalling 2025–2026 DBX and 2026 DBX S vehicles; TPMS warning light may not illuminate for low tire pressure.
FDA•MODERATEBombay Kitchen Tikka SevBombay Kitchen Tikka Sev is recalled due to undeclared FD&C Yellow #6 and FD&C Red #40 food dyes.
3 products
FDA•MODERATEFluocinonide 0.05% CreamTaro Pharmaceuticals is recalling Fluocinonide 0.05% Cream due to out-of-specification viscosity results.
3 products
FDA•MODERATEOxoid Salmonella 9-O Agglutinating SeraRemel Europe is recalling Oxoid Salmonella 9-O Agglutinating Sera due to potential cross-reactivity and misidentification risks.
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 potential premature failure of the lock levers.
12 products
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 do not meet standard manufacturing specifications.
2 products
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•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 inaccurate antimicrobial susceptibility testing results.
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 the HF-OCT Imaging System (Model G10-01) to address a software issue that may cause inaccurate length 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 due to unauthorized configuration changes that deviate from validated settings.
FDA•MODERATEHiResolution Bionic Ear System M Zn-Air Battery PakAdvanced Bionics is recalling M Zn-Air Battery Paks for cochlear implants due to a non-compliant battery door design.
2 products
FDA•MODERATETangent Single Use Digital CatheterTangent Endoscopy is recalling single-use digital catheters due to a risk of fractures at the distal shaft tip.
FDA•MODERATEVancomycin HCl InjectionFagron is recalling Vancomycin HCl 1.5g/250mL injection due to sterility concerns and a potential detachment of the administration port 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 recalled due to manufacturing facility inspection 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•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 between 5mm and 6mm sizes.
2 products