All Recalls

Daimler Coaches is recalling 2009–2020 Setra S417 and 2012–2019 S407 buses due to dashboard switch illumination failures that may distract drivers.

Hino 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.

Booey's Dragon's Breath sauce is recalled for undeclared fish (anchovy) and sesame allergens.

Gentuity is correcting the HF-OCT Imaging System (Model G10-01) to address a software issue that may cause inaccurate length measurements.

Olympus is recalling Thunderbeat II Shears (Model TB2-0520FC) due to the risk of a distal tip component detaching during use.

Hologic is correcting Genius Review Station displays due to unauthorized configuration changes that deviate from validated settings.

Advanced Bionics is recalling M Zn-Air Battery Paks for cochlear implants due to a non-compliant battery door design.

Tangent Endoscopy is recalling single-use digital catheters due to a risk of fractures at the distal shaft tip.

Fagron is recalling Vancomycin HCl 1.5g/250mL injection due to sterility concerns and a potential detachment of the administration port part.

Mercedes-Benz is recalling 2026 GLC models with center rear seat belts that may fail to properly restrain child seats.

Hyundai 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.

Altec 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.

Grand Design is recalling 2025–2026 Lineage motorhomes; entry steps may deploy while in transit, increasing crash risk.

Braun is recalling 2023–2024 Ram ProMaster vehicles with incorrect emergency exit window glass that fails FMVSS 226 safety standards.

Kia is recalling 2027 Telluride Hybrid second-row power seats that may fail to detect and stop for a person.

Exchange Select Honey Lemon Cough Drops are recalled due to manufacturing facility inspection observations that may impact product quality.

Leading Pharma is recalling Furosemide Tablets 80 mg (NDC 69315-118-01) due to N-nitroso-Furosemide above recommended limits.

Foundation Medicine is recalling Sequencing Agent SEQ0067 component of FoundationOne CDx due to possible false-positive BARD1 variants.

Bee Well Honey Farm & Supply is recalling Wildflower Honey in 12 oz, 22 oz, and 44 oz sizes due to high C4 sugar content.

Centinel Spine is recalling Prodisc C SK U.S. cervical disc implants due to a labeling mix-up between 5mm and 6mm sizes.

Frigidaire is recalling 23 gas range models (serials VF52200000–VF54399999) due to delayed oven ignition posing a burn hazard.

Amazon Basics Camping Folding Pocket Knife (model B0DM5BJK3H) recalled due to blade mechanism failure and laceration hazard.

Tainoki is recalling office chairs (models M7016O, M7004O, M7074O) with bases that can bend, creating a fall hazard.

Goregent infant walkers (Model 901) sold on Amazon violate safety standards and pose fall hazards.

Aisstxoer model GH018L adult helmets (size large, pink) fail mandatory safety standards and may not protect in a crash.

Specialized is recalling Turbo Como SL e-bike forks (2021–2026) due to fatigue crack risk causing fall hazard.

Wagner is recalling 900 Series power steamers (models 905e, 915e, 925e) due to burn hazard from hot hose and water expulsion.

BUILT LUUM light up tumblers (16–18 oz) recalled due to breakage exposing button cell batteries; choking and ingestion hazard to children.

Riverence is recalling Smoked Trout Dip due to an undeclared milk allergen.

Amneal is recalling tramadol 50 mg tablets (NDC 60219-2348-5) due to elevated N-nitroso-desmethyl-tramadol impurity.

Teva Pharmaceuticals is recalling Clonidine Transdermal System 0.2 mg/day due to the use of an unapproved raw material during manufacturing.

International is recalling 2023–2027 IC Bus CESB and 2025–2027 EVSB school buses over insufficient epoxy on body panel joints that may separate in a crash.

Terex is recalling 2019–2026 General 65, 80, 95, C4000, C5000, C6000 digger trucks; pole guide arm may fall due to cracked weld.

Lippert is recalling certain 8K axles with incorrect seals that can cause oil leakage, bearing failure, and wheel loss.

GM is recalling 2018–2019 Silverado and Sierra Crew Cab trucks over roof rail air bag inflator end cap detachment or rupture risk.

Ford is recalling certain 2022–2025 Lincoln Navigator, Nautilus, Aviator, and Explorer vehicles over Image Processing Module resets causing loss of rearview camera and ADAS features.

Integra LifeSciences is recalling Cytal Wound Matrix 2-Layer 5x5 cm dressings due to out-of-specification endotoxin results.

Philips is recalling AneurysmFlow software due to unreliable MAFA ratio data that may lead to incorrect clinical decisions.

Elekta is recalling the Leksell Vantage Arc System due to a defect in the locking mechanism that may cause coordinate shifting during procedures.

Medline is recalling various neuro sponges due to higher-than-expected endotoxin levels.

DJO is recalling the IceMan Classic3 cold therapy unit (Model 11-0494) due to a broken connector that may interrupt cold therapy.

Toyota is recalling Lexus NX350, NX250, RX350, and TX350 vehicles over rearview camera display failure that reduces rear visibility.

Land Rover is recalling 2026 Defender vehicles with defective third-row seat belt anchorage welds that may fail to restrain occupants.

Keystone is recalling 2026 Montana fifth wheel trailers due to improperly secured wiring that may be damaged by the bedroom slide-out, creating fire risk.

Diversatek Healthcare is recalling the Viper 3-Stage Fixed Wire Balloon Dilator due to incorrect labeling of balloon sizes and pressures.

Alembic Pharmaceuticals is recalling Bromfenac Ophthalmic Solution 0.07% (NDC 62332-583-03) due to failed impurities and degradation specifications.

Island Kinetics is recalling Remedy Gel hydrocortisone 1% due to subpotency.

Siemens is recalling Dimension Creatinine Flex reagent cartridges (lots GA6307, BA7005) due to potential imprecision in patient creatinine results.

Teva is recalling Octreotide Acetate for Injectable Suspension due to a lack of assurance of sterility.

Chiesi USA is recalling Curosurf 240 mg intratracheal suspension vials (NDC 10122-510-03) due to lack of sterility assurance.