Device Recall
FDA•MODERATE
B. Braun Cesk Northside Anesthesia Tray
B. Braun is recalling the Cesk Northside Anesthesia Tray (Model 555076) due to potential cracking of the included adhesive tubing.
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FDA•CRITICALFrozen Fish BallsFrozen Fish Balls are being recalled due to undeclared wheat and sesame allergens.
3 products
FDA•CRITICALWhy Not Natural Moringa CapsulesWhy Not Natural is recalling Moringa Capsules due to potential Salmonella contamination.
FDA•MODERATEJiffy Original Composite Polisher Cups (Coarse)Ultradent is recalling Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011, due to crumbling and breakage risk.
FDA•MODERATEMedline Medcrest Surgical GownsMedline is recalling Medcrest surgical gowns due to a risk of fabric delamination during laundering, which may lead to infection.
3 products
NHTSA•MODERATEZero Motorcycles Front Brake HoseZero Motorcycles is recalling 2024–2025 DSR/X, DS, DSR, and DSRP motorcycles; front brake hose may leak, reducing braking ability.
NHTSA•MODERATEDucati Streetfighter V4 and Panigale V4 Rear Brake HoseDucati is recalling 2025–2026 Streetfighter V4 and Panigale V4 motorcycles due to rear brake hose damage from excessive heat.
NHTSA•MODERATEToyota Prius Rear Door LatchToyota is recalling 2023–2026 Prius models over rear door latch defect that may allow doors to open unexpectedly.
FDA•CRITICALHycoat Hyaluronate Sodium Sterile SolutionNeogen is recalling Hycoat Hyaluronate Sodium Sterile Solution for veterinary use due to potential microbial contamination.
2 products
FDA•MODERATEFrozen Half Shell OystersKhee Trading is recalling frozen half shell oysters due to potential Norovirus contamination.
FDA•MODERATEDiclofenac Sodium Topical Gel 3%Taro Pharmaceuticals is recalling Diclofenac Sodium Topical Gel 3% (100 g) due to viscosity specification failure.
FDA•CRITICALImpella RP Flex with SmartAssistAbiomed is recalling Impella RP Flex with SmartAssist devices due to a potential malfunction of the differential pressure sensor.
3 products
FDA•MODERATEBD 10mL Non-Sterile Luer-Lok SyringeBD is recalling 10mL non-sterile Luer-Lok syringes (catalog 301029) due to incorrect Luer Slip syringes mixed into batches.
FDA•MODERATELutronic CLARITY II Laser SystemLutronic is recalling CLARITY II Laser System (Model 1110200210) due to sparking and burn hazard.
NHTSA•MODERATEHyundai Instrument Panel DisplayHyundai is recalling 2025–2026 Tucson, IONIQ 5, Santa Cruz, Kona, Palisade, Santa Fe, and Sonata vehicles over instrument panel display failure.
NHTSA•MODERATEKia Instrument Panel DisplayKia is recalling 2025–2026 K4, Sorento, Sportage, K5, EV9, and Carnival vehicles due to instrument panel display failure that may hide speedometer and warning lights.
FDA•MODERATEKeto-C Antiseptic WipesStratford Care USA is recalling Keto-C Antiseptic Wipes (50ct) due to misbranding; product contains non-medicated otic flush instead of labeled antiseptic.
36 products
FDA•MODERATERepackaged M&Ms Peanut CandiesBeacon Promotions is recalling 1.3 oz repackaged M&Ms Peanut candies due to undeclared milk, soy, and peanut allergens.
3 products
FDA•MODERATEGerber Arrowroot BiscuitsGerber Arrowroot Biscuits (5.5 oz, UPC 015000005962) recalled for potential paper/plastic contamination in arrowroot flour.
FDA•MODERATEAsteria Health Testosterone Sterile PelletsAsteria Health is recalling 100 mg testosterone pellets due to potential metal particulate contamination.
25 products
FDA•MODERATETrazodone Hydrochloride 50 mg TabletsGranules Pharmaceuticals is recalling Trazodone Hydrochloride 50 mg tablets (NDC 70010-231-01) due to foreign tablets or capsules in bottles.
FDA•MODERATESodium Iodide (I-131) Therapeutic Oral SolutionRadnostix is recalling Sodium Iodide (I-131) Therapeutic Oral Solution due to the presence of particulate matter.
FDA•MODERATEPhilips Azurion 7 M12 SystemPhilips is recalling Azurion 7 M12 systems due to a risk of unexpected table movement when the Reset Geometry button is pressed.
8 products
NHTSA•MODERATEGrand Design Momentum and Solitude Fifth Wheel U-BoltGrand Design is recalling 2021–2024 Momentum and 2022–2024 Solitude Fifth Wheel trailers over loose U-bolts that may shift the axle.
NHTSA•MODERATEColeman Travel Trailer Murphy BedKeystone is recalling 2026 Coleman travel trailers; murphy bed brackets may not be secured, risking unexpected bed collapse.
FDA•CRITICALRaaw Energy Dog Food Chicken MedleyRaaw Energy is recalling Dog Food Chicken Medley (2-lb and 5-lb tubes) due to Listeria, Salmonella, and Campylobacter contamination.
5 products
FDA•MODERATETops GOLD PicklesMangalm LLC is recalling Tops GOLD pickle products due to potential erucic acid contamination from mustard oil.
6 products
FDA•CRITICALNavitas Organics Organic Chia SeedsNavitas Organics is recalling 8 oz packages of Organic Chia Seeds due to potential Salmonella contamination.
FDA•MODERATEI.T.S. Headless Compression Screw SystemI.T.S. is recalling its Headless Compression Screw System due to updated MRI safety testing showing higher temperature risks.
24 products
FDA•MODERATEDatascope CS300 IABPDatascope is updating the IFU for CS300 IABP software version C.01 to correct battery runtime and cycle specifications.
2 products
NHTSA•MODERATEToyota Tundra Panoramic View MonitorToyota is recalling 2024–2025 Tundra vehicles with Panoramic View Monitor systems due to rearview camera display failure.
NHTSA•MODERATEForest River Recreational Trailer 7-Way ConnectorForest River is recalling 2026 Cascade, Cherokee, and Campsite Reserve trailers with 7-way connectors lacking over-current protection, posing a fire risk.
NHTSA•MODERATEGrand Design Lineage Solar PanelGrand Design is recalling 2025–2026 Lineage RVs; solar panels may detach due to adhesive failure.
2 products
NHTSA•MODERATEToyota bZ4X Rear Combination Light AssemblyToyota is recalling rear combination light assemblies (part nos. 81561-42290, 81551-42290) for bZ4X vehicles due to missing side marker lights, increasing crash risk.
NHTSA•MODERATECollins Bus School Bus Body PanelsForest River Bus is recalling 2026 Collins Bus school buses with incorrectly attached body panels that may separate in a crash.
- NHTSA•MODERATEForest River Collin Bus Body Panels
Forest River is recalling 2026 Collin Bus transit buses with body panels that may separate due to incorrectly applied adhesive.
NHTSA•MODERATEBrinkley Model Z Trailer Shore Power InletBrinkley is recalling 2026 Model Z trailers with improperly tightened shore power inlet lugs that may overheat and cause fire.
NHTSA•MODERATEHyundai Palisade Side Curtain Air BagHyundai is recalling 2020–2025 Palisade vehicles over improper third-row side curtain air bag deployment in crashes.
NHTSA•MODERATEPolestar 3 Rear Seat BackrestPolestar is recalling 2025 Polestar 3 vehicles with loose rear seat backrest striker brackets that may fail in a crash.
NHTSA•MODERATEFWMOTO FLY-10 Scooter Brake SystemFWMOTO is recalling 2022–2024 FLY-10 and FLY E-BIKE FLY-10 scooters over insufficient brake pad performance.
- NHTSA•MODERATEFWMOTO FLY-10 Scooter Rear Wheel Hub
FWMOTO is recalling 2022–2024 FLY-10 scooters with rear wheel hubs missing DOT markings, raising crash risk.
FDA•MODERATERed Button Movie House PopcornLee's Commissary is recalling Red Button Movie House Popcorn due to potential foreign material contamination.
NHTSA•MODERATEBlue Bird Vision Transit Bus WindowsBlue Bird is recalling one 2026 Vision transit bus with illegible DOT markings on windows.
NHTSA•MODERATEBlue Bird School Bus WindowsBlue Bird is recalling 2026–2027 Vision and All American school buses with illegible DOT window markings.
NHTSA•MODERATEChevrolet Blazer EV Parking Brake Wiring HarnessGM is recalling 2024–2025 Chevrolet Blazer EV vehicles for damaged parking brake wiring harness that may cause unintended activation or loss of function.
FDA•MODERATEBisoprolol Fumarate and Hydrochlorothiazide Tablets 2.5 mg/6.25 mgUnichem Pharmaceuticals recalls Bisoprolol/Hydrochlorothiazide 2.5/6.25 mg tablets (NDC 29300-187-01) due to N-Nitroso Bisoprolol impurity specification failure.
FDA•LOWDoxazosin Tablets, USP 4 mgUnichem is recalling Doxazosin Tablets 4 mg (NDC 29300-353-10) due to incorrect tablet imprinting that may cause medication errors.
FDA•MODERATEAuris Health MONARCH Platform Bronchoscopy SystemAuris Health is recalling MONARCH Platform Bronchoscopy systems due to a software issue that may cause unexpected robotic arm repositioning and contact with the patient.
FDA•MODERATEEVO+ Visian Toric Implantable Collamer Lens (TICL)Staar Surgical is recalling EVO+ Visian Toric ICL Model VTICM5 due to incorrect length labeling (12.1 mm labeled vs. 12.6 mm actual) causing excessive vault and potential angle closure.
FDA•MODERATEPhysio-Control Infant/Child Defibrillator ElectrodesPhysio-Control is recalling infant/child defibrillator electrodes due to a risk of delamination that may prevent proper therapy delivery.
2 products