Device Recall
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Olympus ViziShot 2 FLEX EBUS-TBNA Needles
Olympus is recalling ViziShot 2 FLEX (19G) EBUS-TBNA needles due to a device safety defect.
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FDA•Genova Yellowfin TunaGenova Yellowfin Tuna is recalled due to potential Clostridium botulinum contamination, which can cause serious illness.
FSIS•CRITICALSuzanna's Kitchen Ready-To-Eat Grilled Chicken Breast FilletsSuzanna's Kitchen recalls 13,720 lbs of ready-to-eat grilled chicken breast fillets (lot 60104 P1382 287 5 J14) over possible Listeria contamination.
FDA•MODERATEPremium Food Jordan AlmondsPremium Food Jordan Almonds are recalled for undeclared wheat and color additives.
2 products
FDA•MODERATESimply Nature Spinach BitesDr. Praeger's is recalling Simply Nature Spinach Bites (12 oz) due to possible rodent hair contamination.
FDA•MODERATEWoodland Gourmet Arrowroot FlourWoodland Gourmet Arrowroot Flour is being recalled due to the potential presence of foreign material.
FDA•CRITICALUDENYCA Pegfilgrastim-cbqv InjectionUDENYCA pegfilgrastim-cbqv prefilled syringes (Lot 2199821) recalled due to improper storage temperature.
FDA•MODERATEThyroid, USPSpecialty Process Labs is recalling Thyroid, USP (NDC 81305-100-02) due to subpotency.
FDA•MODERATEMediHoney Gel DressingIntegra LifeSciences is recalling MediHoney Gel dressings (catalog numbers 31805 and 31815) due to a potential sterile barrier breach.
3 products
FDA•CRITICALOlympus High Flow Insufflation UnitOlympus is recalling the High Flow Insufflation Unit, Model UHI-3, due to a software issue that may lead to overpressure events.
3 products
FDA•MODERATEGE Healthcare Centricity Universal Viewer Zero Footprint ClientGE Healthcare is recalling Centricity Universal Viewer Zero Footprint Client (Models 2110344-039, -046, -047) due to patient information and image mismatch risk.
NHTSA•MODERATELucid Gravity Rearview CameraLucid is recalling 2025–2026 Gravity vehicles where the rearview camera may not display in reverse, reducing rear visibility.
NHTSA•MODERATELucid Air Rearview CameraLucid is recalling 2022–2026 Air vehicles with AD02 package; rearview camera may not display in reverse.
NHTSA•MODERATEGenesis G80, GV80, GV60, GV70 Instrument Panel DisplayHyundai is recalling 2025–2026 Genesis G80, GV80, GV60, GV70 vehicles for instrument panel display failure that may hide speedometer and fuel gauge.
NHTSA•MODERATEForest River Freelander Solar Panel WiringForest River is recalling 2026 Freelander motorhomes over solar panel wiring lacking over-current protection, creating a fire risk.
NHTSA•MODERATEWinnebago Motorhome Water Tank Heating PadWinnebago is recalling motorhomes with ThermaHeat Tank Pads that may fail and pose a fire risk.
NHTSA•MODERATELippert Bus WindowsLippert is recalling bus windows with illegible DOT markings that may be replaced with incorrect glass type.
NHTSA•MODERATEForest River Trans Tech School BusForest River is recalling 2025–2026 Trans Tech school buses with modified seating that may exceed rear axle weight limits, risking loss of control.
NHTSA•MODERATENewmar Freedom Aire Water Tank Heating PadNewmar is recalling 2026 Freedom Aire motorhomes with ThermaHeat Tank Pad due to fire risk from heating pad failure.
FDA•Live it Up Super GreensLive it Up is recalling Super Greens Original and Wild Berry pouches and packs due to potential Salmonella contamination.
FDA•MODERATEAonic Complete Hers Dietary SupplementAonic Complete Hers dietary supplement shots are recalled due to potential E. coli, coliform, and Pseudomonas aeruginosa contamination.
2 products
FDA•CRITICALLive it Up Super Greens Dietary SupplementLive it Up Super Greens dietary supplement is recalled due to potential Salmonella Typhimurium contamination.
4 products
FDA•LOWLubna Quality Products Mung BeansLubna Quality Products is recalling 4 lb mung bean packages due to unapproved pesticide (Thiamethoxam) contamination.
FDA•MODERATEWinCo Foods Deli Margherita PizzaWinCo Foods is recalling Deli Margherita Pizza Thin Crust due to potential metal fragment contamination.
FDA•MODERATEMethylprednisolone Tablets USP Dosepak 4 mgGreenstone is recalling methylprednisolone 4 mg tablets (NDC 59762-4440-2) due to incorrect blister foil orientation causing incorrect dosing information.
FDA•MODERATEReverse Shoulder Prosthesis Humeral Socket InsertEncore Medical is recalling the RSP Humeral Socket Insert (model 509-00-432) due to incorrect product labeling.
3 products
FDA•MODERATEAesculap Minop TrocarAesculap is recalling the Minop Trocar 150mm (Model FF399R) due to a potential defect where the trocar shaft length may be too long.
FDA•MODERATEMedline Unna-Z Stretch Zinc Paste BandageMedline is recalling Unna-Z Stretch Zinc Paste Bandages due to a labeling error omitting castor oil and calamine ingredients.
CPSC•Adams RealComfort and StyleWell Adirondack Patio ChairsAdams RealComfort and StyleWell Adirondack chairs (model ML837-15, August 2025) recalled for crack and collapse hazard.
CPSC•Morgan Lane Asher Pajama SetsMorgan Lane Asher Pajama Sets (Style 816TR, sizes 2T–14) recalled for violating flammability standards; risk of serious burn injury.
CPSC•Greatale Self-Feeding PillowsGreatale self-feeding pillows pose aspiration and suffocation risk; sold on Amazon Sept. 2024–July 2025.
CPSC•Energizer Large Power Indicator LanternEnergizer is recalling Large Power Indicator Lanterns (model BGAAL9, June 2024 date code) due to lithium-ion battery overheating and burn hazard.
CPSC•HEZI Brand Power StripsHEZI power strips with gray or yellow metal enclosures recalled over electrocution hazard from ungrounded metal casing.
CPSC•BBWOO Baby LoungersBBWOO baby loungers (models BLG26BE, BLG23BD, BLG04BD, and others) recalled for low sides, wide foot openings, and lack of stand posing fall and entrapment hazards to infants.
CPSC•Frigidaire MinifridgeFrigidaire minifridges (models EFMIS121, EFMIS129, EFMIS137, EFMIS149, EFMIS175) recalled over fire and burn hazards from electrical short circuits.
CPSC•Ruahouine Hair Growth Serum BottlesRuahouine Hair Growth Serum (60ml) recalled for non-child-resistant packaging; minoxidil poses poisoning risk to children.
CPSC•RootStim Beard Growth Serum Spray BottlesRootStim Beard Growth Serum spray bottles (5% minoxidil) recalled for non-compliant child-resistant packaging; risk of poisoning to children.
CPSC•R.X.Y Adult Bicycle HelmetsR.X.Y adult bike helmets (Kx012) sold on Amazon fail mandatory safety standards and may not protect against head injury in a crash.
CPSC•KEAWIS Crib MattressesKEAWIS crib mattresses (Model XX-BM-01) recalled for entrapment and suffocation risk due to improper fit in some cribs.
NHTSA•MODERATEFord Engine Block HeaterFord is recalling 2016–2018 Focus and 2019–2024 Explorer vehicles; engine block heater may short circuit and cause fire.
NHTSA•MODERATEFord Engine Block HeaterFord is recalling 2013–2019 Focus, Escape, and MKC vehicles with 2.0L engines over engine block heater fire risk.
NHTSA•MODERATEFord Engine Block HeaterFord is recalling engine block heaters (CV6Z-6A051-CA, CV6Z-6A051-AA) for 2013–2019 Ford/Lincoln 2.0L vehicles due to short-circuit fire risk.
NHTSA•CRITICALGulf Stream Trail Boss and Ameri-Lite Rear Turn SignalsGulf Stream is recalling 2026 Trail Boss and Ameri-Lite trailers with reversed turn signal wires that activate opposite to driver intent.
NHTSA•MODERATERivian R1T and R1S Seat Belt RetractorRivian is recalling 2022–2025 R1T and 2022–2026 R1S vehicles over improperly tightened second-row seat belt retractor bolts.
FDA•Spring & Mulberry Chocolate BarsSpring & Mulberry is recalling various chocolate bar flavors due to potential Salmonella contamination.
FDA•MODERATEMargarita Thin Crust PizzaRose and Shore is recalling Margarita Thin Crust Pizzas due to potential metal contamination in the tomato ingredient.
FDA•MODERATESpicely Organic Garlic SaltSpicely Organic Garlic Salt is recalled due to undeclared salt in the product.
3 products
FDA•MODERATESevillo Fine Foods Slow Roasted Diced TomatoesSevillo Fine Foods is recalling 24 lb bulk boxes of frozen Slow Roasted Diced Tomatoes due to potential metal fragment contamination.
2 products
FDA•MODERATEOxycodone Hydrochloride Tablets, USP 5 mgAmerican Health Packaging is recalling Oxycodone Hydrochloride 5 mg tablets due to defective blister card seals that allow tablets to fall out.
FDA•MODERATEPIE PAK Trolley SystemEdermy is recalling PIE PAK trolley systems (models P2HC-A, P2HC-S, P2HC) due to a lack of required 510(k) clearance.
2 products