NHTSA•MODERATE
Newmar Freedom Aire Water Tank Heating Pad
Newmar is recalling 2026 Freedom Aire motorhomes with ThermaHeat Tank Pad due to fire risk from heating pad failure.
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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•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.
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•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•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
FDA•MODERATESpicy Breakfast BurritoMG Foods is recalling 10 oz Spicy Breakfast Burritos due to potential contamination with small hard plastic fragments.
FDA•MODERATEOctopus Nuvo Tissue StabilizerMedtronic is recalling Octopus Nuvo Tissue Stabilizer (TSMICS1) due to incorrect tubing assembly that may affect surgical tissue stabilization.
FDA•MODERATELaerdal Compact Suction Unit 4 RTCALaerdal is recalling Compact Suction Unit 4 RTCA models due to potential electromagnetic noise interference exceeding safety standards.
NHTSA•MODERATEEast Trailers Beast Rear Impact GuardEast Trailers is recalling 2024–2026 Beast trailers; rear impact guard may detach due to improper weld.
NHTSA•MODERATELippert 3000 Series Hidden Hinge Ramp DoorLippert 3000 Series Hidden Hinge Ramp Doors may break away from the frame during use, posing an injury risk.
FDA•MODERATESpectrum IQ Infusion PumpBaxter is recalling Spectrum IQ Infusion Pumps (Model 3570009) because they were released without full occlusion alarm testing.
FDA•MODERATESonic Tots Frozen PotatoesMcCain Foods is recalling Sonic Tots frozen potato products due to potential contamination with small hard plastic fragments.
2 products
FDA•MODERATEIsotretinoin 40 mg CapsulesTeva is recalling Isotretinoin 40 mg capsules due to superpotency and subpotency concerns that may affect treatment efficacy or safety.
2 products
FDA•MODERATEEndo-Model Knee Implant PlateauWaldemar Link is recalling the Endo-Model Replacement Plateau due to a risk of fracture that may cause the bushing to detach.
13 products
NHTSA•MODERATETerex Areal Device Control ValveTerex is recalling 2025 TL-Series, LT-Series, LTM40, HR40, HR46, and SCM55 areal devices with overheating hydraulic control valves.
FDA•MODERATEFurosemide Tablets USP 40 mgRising Pharmaceuticals is recalling Furosemide Tablets 40 mg (NDC 64980-563-10) due to foreign substance contamination.
FDA•MODERATESea Moss Gel SuperfoodDiva Fam is recalling Sea Moss Gel Superfood due to potential Clostridium botulinum contamination.
14 products
FDA•MODERATEAPTUS 2.5 TriLock Screw 16mmMedartis is recalling APTUS 2.5 TriLock Screw 16mm (Model A-5750.16/1) due to a packaging mix-up with 2.8mm screws.
2 products
FDA•MODERATEMaquet Venous Bubble SensorMaquet is recalling Venous Bubble Sensors for 3/8" x 3/32" tubing due to cable durability issues that may cause sensor failure.
NHTSA•MODERATE2026 Range Rover Sport Certification LabelLand Rover is recalling 2026 Range Rover Sport vehicles with incorrect weight information on the certification label, increasing crash risk.
NHTSA•MODERATECooper Discoverer SRX TiresGoodyear is recalling Cooper Discoverer SRX 255/50R20 tires with incorrect Tire Identification Numbers.
FDA•MODERATEFDR Visionary Suite X-ray GeneratorFDR Visionary Suite X-ray generators are being recalled due to a risk of overheating and smoke caused by faulty electromagnetic contactors.
FDA•MODERATEDiowave 250W Laser SystemDiowave 250W Laser System recalled; software update needed to correct power output exceeding FDA-cleared 60W limit.
FDA•MODERATESmoked Grouper DipIsland Crab Corporation is recalling Smoked Grouper Dip due to undeclared milk, eggs, and sodium metabisulfite.
FDA•MODERATEMedline Kits with Tego ConnectorsMedline is recalling kits with Tego Connectors due to seal defects that may cause fluid leakage, therapy delays, or contamination risks.
6 products
FDA•MODERATEOlympus ShockPulse-SE Lithotripsy System GeneratorOlympus is recalling ShockPulse-SE Lithotripsy System generators due to a mis-wired component that may cause treatment delays.
2 products
FDA•MODERATEGluten Free Seasoned Vegan Pizza CrustRich Products Corp is recalling Gluten Free 14" Seasoned Vegan Pizza Crust due to undeclared milk and egg allergens.
2 products
FDA•MODERATEHannaford Hamburger Dill Pickle ChipsHannaford hamburger dill pickle chips (UPC 0 41268 14889 9) recalled due to glass contamination.
FDA•MODERATEOlympus Single Use 3-Lumen Sphincterotome VOlympus is recalling the Single Use 3-Lumen Sphincterotome V due to a manufacturing defect that may cause the device to deform and lose function.
30 products
FDA•MODERATEMedline Convenience KitsMedline is recalling various surgical and biopsy convenience kits due to potential issues with sterilization and packaging equipment calibration.
62 products
FDA•MODERATEPhilips Brilliance iCT Gantry Rotor FastenersPhilips is recalling Brilliance iCT CT systems because loose gantry rotor fasteners could cause parts to become unsecured or expelled.
4 products
NHTSA•MODERATEAptany Eco Sendero M/T2 TireWanli is recalling Aptany Eco Sendero M/T2 tires (LT265/75R16) due to sidewall separation risk.
- Device RecallFDA•MODERATEMint Lesion Software
Mint Medical is recalling Mint Lesion software versions 3.4.0–3.9.5 due to a risk of data loss or incorrect patient linking.
FDA•MODERATEMedline Convenience KitsMedline is recalling convenience kits due to potential issues with the sterilization process that may affect product sterility.
58 products
FDA•MODERATEKarison PanjiriKarison is recalling Panjiri due to an undeclared milk allergen.
5 products
FDA•MODERATEPrismaflex M100 SetVantive is recalling the Prismaflex M100 Set due to a potential dislodgement of the deaeration chamber from the control unit.
8 products
NHTSA•MODERATEBlue Bird Vision and All American Bus Wheelchair RestraintBlue Bird is recalling 2026 Vision and All American buses with QRT-Deluxe and QRT-Max wheelchair restraints that may not lock.
FDA•MODERATEAQ 120 GFEW Aquarion Preserved CartridgesEncon Safety Products is recalling AQ 120 GFEW Aquarion Preserved Cartridges due to cGMP manufacturing deviations.
FDA•MODERATEVITEK 2 Gram-negative Susceptibility CardsBioMérieux is recalling 30+ VITEK 2 susceptibility card variants over risks of quality control failures and false resistant test results.
2 products