All Recalls

Khee Trading is recalling frozen half shell oysters due to potential Norovirus contamination.

Taro Pharmaceuticals is recalling Diclofenac Sodium Topical Gel 3% (100 g) due to viscosity specification failure.

BD is recalling 10mL non-sterile Luer-Lok syringes (catalog 301029) due to incorrect Luer Slip syringes mixed into batches.

Lutronic is recalling CLARITY II Laser System (Model 1110200210) due to sparking and burn hazard.

Hyundai is recalling 2025–2026 Tucson, IONIQ 5, Santa Cruz, Kona, Palisade, Santa Fe, and Sonata vehicles over instrument panel display failure.

Kia 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.

Stratford Care USA is recalling Keto-C Antiseptic Wipes (50ct) due to misbranding; product contains non-medicated otic flush instead of labeled antiseptic.

Beacon Promotions is recalling 1.3 oz repackaged M&Ms Peanut candies due to undeclared milk, soy, and peanut allergens.

Gerber Arrowroot Biscuits (5.5 oz, UPC 015000005962) recalled for potential paper/plastic contamination in arrowroot flour.

Asteria Health is recalling 100 mg Testosterone sterile pellets due to the potential presence of metal particulate matter.

Granules Pharmaceuticals is recalling Trazodone Hydrochloride 50 mg tablets (NDC 70010-231-01) due to foreign tablets or capsules in bottles.

Radnostix is recalling Sodium Iodide (I-131) Therapeutic Oral Solution due to the presence of particulate matter.

Philips is recalling Azurion 3 and 7 M12 systems over a software defect that can cause unexpected patient table movement.

Grand Design is recalling 2021–2024 Momentum and 2022–2024 Solitude Fifth Wheel trailers over loose U-bolts that may shift the axle.

Keystone is recalling 2026 Coleman travel trailers; murphy bed brackets may not be secured, risking unexpected bed collapse.

Mangalm is recalling Tops GOLD pickle products due to potential erucic acid contamination from mustard oil.

I.T.S. is recalling the Headless Compression Screw System due to higher-than-expected temperature increases during MRI procedures.

Datascope is updating the IFU for CS300 IABP software version C.01 to correct battery runtime and cycle specifications.

Toyota is recalling 2024–2025 Tundra vehicles with Panoramic View Monitor systems due to rearview camera display failure.

Forest River is recalling 2026 Cascade, Cherokee, and Campsite Reserve trailers with 7-way connectors lacking over-current protection, posing a fire risk.

Grand Design is recalling 2025–2026 Lineage RVs; solar panels may detach due to adhesive failure.

Toyota is recalling rear combination light assemblies (part nos. 81561-42290, 81551-42290) for bZ4X vehicles due to missing side marker lights, increasing crash risk.

Forest River Bus is recalling 2026 Collins Bus school buses with incorrectly attached body panels that may separate in a crash.

Forest River is recalling 2026 Collin Bus transit buses with body panels that may separate due to incorrectly applied adhesive.

Brinkley is recalling 2026 Model Z trailers with improperly tightened shore power inlet lugs that may overheat and cause fire.

Hyundai is recalling 2020–2025 Palisade vehicles over improper third-row side curtain air bag deployment in crashes.

Polestar is recalling 2025 Polestar 3 vehicles with loose rear seat backrest striker brackets that may fail in a crash.

FWMOTO is recalling 2022–2024 FLY-10 and FLY E-BIKE FLY-10 scooters over insufficient brake pad performance.

FWMOTO is recalling 2022–2024 FLY-10 scooters with rear wheel hubs missing DOT markings, raising crash risk.

Red Button Movie House Popcorn is being recalled due to the potential presence of foreign material.

Blue Bird is recalling one 2026 Vision transit bus with illegible DOT markings on windows.

Blue Bird is recalling 2026–2027 Vision and All American school buses with illegible DOT window markings.

GM is recalling 2024–2025 Chevrolet Blazer EV vehicles for damaged parking brake wiring harness that may cause unintended activation or loss of function.

Unichem Pharmaceuticals recalls Bisoprolol/Hydrochlorothiazide 2.5/6.25 mg tablets (NDC 29300-187-01) due to N-Nitroso Bisoprolol impurity specification failure.

Auris Health is recalling MONARCH Platform Bronchoscopy systems due to a software issue that may cause unexpected robotic arm repositioning and contact with the patient.

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.

Physio-Control is recalling infant/child defibrillator electrodes due to a risk of delamination that may prevent proper therapy delivery.

Stryker is updating the MOLLI 2 System labeling due to the risk of magnetized surgical tools dislodging markers during tissue removal.

Agiliti is recalling Adapt Pump Model 61600200 due to Microclimate Management function failure after Autofirm use.

Volkswagen is recalling 2023–2025 ID.4 vehicles over high-voltage battery overheating and fire risk.

Alexis Fire is recalling 2022–2024 Freightliner M2 tanker trucks over loose axle clamp fasteners risking loss of control.

Nissan is recalling 2025–2026 Altima, Sentra, Frontier, and Kicks over improperly welded door strikers that may open while driving.

Ford is recalling 2025 F-59 and F-53 vehicles; brake lights may fail to illuminate due to an incorrectly installed switch.

Oshkosh is recalling 2025 NGDV vehicles; rear axle hub fasteners may loosen and cause wheel detachment.

Ford is recalling 2026 Explorer vehicles with improperly bonded windshields that may detach in a crash.

Keystone is recalling 2024–2026 Fuzion, Raptor, Redwood, and Voltage travel trailers; ramp door may break during use.

Garcia Nevett is recalling Crunchy Caramel dark chocolate bars due to an undeclared milk allergen.

Acme United is recalling Med Nap BZK Antiseptic Towelettes (NDC 0924-0246-01) due to CGMP deviations.

Instrumentation Laboratory is recalling GEM Premier 5000 PAK cartridges due to errors that may cause cartridge ejection and delayed results.

Roche is recalling cobas pro analytical units due to a software defect causing erroneous, repeated lab results for specific Spline-type assays.