NHTSA•MODERATE
Chevrolet Malibu Rearview Camera
GM recalls 2023–2025 Chevrolet Malibu rearview cameras that may display distorted or blank images.
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NHTSA•MODERATEChevrolet Corvette Rear Turn Signal Warning SystemGM is recalling 2025–2026 Chevrolet Corvette models over a software error that may prevent detection of rear turn signal failure.
NHTSA•MODERATEKeystone Montana Fifth Wheel UnderbellyKeystone is recalling 2026 Montana fifth wheel trailers; underbelly may detach during transit, creating road hazard.
FDA•MODERATESterile Water for Injection USPB. Braun is recalling 3000 mL Sterile Water for Injection USP bags distributed nationwide due to potential sterility and leakage issues.
4 products
FDA•LOWAmprol 25% Medicated ArticleHuvepharma is recalling one bag of Amprol 25% medicated article due to missing lot number and expiration date information.
FDA•MODERATELidocaine HCl Injection 1% 5 mL VialsHuons is recalling Lidocaine HCl injection 1% 5 mL vials due to a lack of assurance of sterility.
9 products
FDA•CRITICALEnoki MushroomsHemu Trading is recalling 150g packages of Enoki Mushrooms due to potential Listeria monocytogenes contamination.
FDA•MODERATEepoc BGEM BUN Test CardSiemens is recalling epoc BGEM BUN Test Cards due to the risk of inaccurate pH and carbon dioxide results that may lead to improper treatment.
FDA•MODERATEPhilips Bridge Prep KitMerit Medical Systems is recalling the Philips Bridge Prep Kit due to potential catheter resistance during use.
4 products
FDA•CRITICALCook Centimeter Sizing CatheterCook is recalling Centimeter Sizing Catheters due to a risk of marker band breakage, which may cause vessel injury or life-threatening harm.
3 products
FDA•MODERATEda Vinci X and Xi Surgical System Universal Surgical ManipulatorIntuitive Surgical is recalling USM arm sub-assemblies for da Vinci X and Xi systems due to a risk of internal screw breakage.
2 products
FDA•MODERATEOne Step 10A In Vitro Diagnostic TestDFI is recalling the One Step 10A in vitro diagnostic test because it was distributed without required FDA premarket clearance or approval.
7 products
FDA•CRITICALRaw Farm Raw CheddarRaw Farm is recalling Raw Cheddar Original cheese due to a multi-state E. coli O157:H7 outbreak.
5 products
FDA•CRITICALMedline Namic Angiographic Control Syringe KitsWindstone Medical is recalling Angio Pack kits containing Medline Namic syringes due to a risk of adapter disconnection and potential injury.
FDA•CRITICALWawa Iced Tea Lemon 16 ozWawa is recalling 16 oz Iced Tea Lemon bottles due to an undeclared milk allergen.
4 products
FDA•Christopher Ranch and Garland Peeled GarlicTops is recalling Christopher Ranch and Garland peeled garlic due to potential Clostridium botulinum contamination.
NHTSA•MODERATEVolvo VNL and VNR Turn Signal SystemVolvo is recalling 2025–2027 VNL and 2026–2027 VNR trucks over turn signal failure risk.
NHTSA•MODERATEAudi 2026 Q3 Sunroof SystemAudi is recalling 2026 Q3 vehicles for sunroof software that allows remote closing without operator visibility.
NHTSA•MODERATEChevrolet Low Cab Forward and Isuzu NRR Wire HarnessIsuzu is recalling 2025–2027 Chevrolet Low Cab Forward and Isuzu NRR vehicles over improperly secured wire harnesses that may chafe, causing engine stall, brake failure, or fire.
NHTSA•MODERATEMack Pioneer and Anthem Trailers Turn SignalMack is recalling 2025–2027 Pioneer and 2027 Anthem trailers with non-functional turn signals that increase crash risk.
FDA•MODERATEEpinephrine Injection USP 1 mg/10mLInternational Medication Systems is recalling Epinephrine Injection 1 mg/10mL (NDC 76329-3318-1) due to lack of sterility assurance.
FDA•MODERATESkin Script Blemish Spot TreatmentSkin Script Blemish Spot Treatment recalled over failed stability specifications; UPC 6 10563 13873 9.
FDA•MODERATEPure Palm Medjool DatesPure Palm is recalling Medjool Dates because they are mislabeled and actually contain Coconut Date Bites.
3 products
FDA•MODERATEPhenylephrine Hydrochloride Injectable SolutionWells Pharma is recalling Phenylephrine Hydrochloride Injectable Solution (40mg, 250mL) due to cGMP deviations.
7 products
FDA•MODERATEi-STAT Blood Gas CartridgesAbbott is recalling i-STAT EG7+, EG6+, and G3+ cartridges due to inaccurate blood gas readings that may lead to incorrect clinical decisions.
3 products
FDA•MODERATEBiofire Spotfire Respiratory/Sore Throat PanelBiofire is recalling the Spotfire Respiratory/Sore Throat Panel due to the risk of false negative results and control failures.
FDA•MODERATEZYMUTEST HIA IgG ELISA KitZYMUTEST HIA IgG ELISA kit lot FD1265 distributed with outdated flyer containing incorrect positive control values.
NHTSA•MODERATERicon R1200 Power Transfer Seat BaseRicon is recalling R1200 series Power Transfer Seat Base units over potential gear motor locking failure.
NHTSA•MODERATEFord Explorer and Mustang Engine Piston CirclipsFord is recalling 2026 Explorer and Mustang vehicles for incorrectly installed piston circlips that may cause engine failure and loss of drive power.
NHTSA•MODERATENova Bus LFS Artic Transit Bus Window GlassNova Bus is recalling 2025 and 2024 LFS Artic transit buses; window glass may detach due to inadequate frame adhesion.
NHTSA•MODERATEToyota Corolla Cross Hybrid Pedestrian Warning SystemToyota is recalling 2023–2025 Corolla Cross Hybrid vehicles for insufficient pedestrian warning sounds in reverse.
NHTSA•MODERATEFord Bronco Sport and Maverick Front Passenger Air BagFord is recalling 2025–2026 Bronco Sport and Maverick vehicles; front passenger air bag may not deploy due to OCS sensor failure.
NHTSA•MODERATEFord Windshield Wiper ArmsFord is recalling 2021–2023 Lincoln Navigator, Expedition, and 2022–2023 F-Series Super Duty trucks due to windshield wiper arm breakage.
- NHTSA•MODERATEFord Lincoln Aviator and Explorer HVAC System
Ford is recalling 2026 Lincoln Aviator and Explorer vehicles for HVAC system failure affecting windshield defrosting.
FDA•LOWMagnesium Chloride 6-Hydrate Crystal 500GAvantor is recalling Magnesium Chloride 6-Hydrate Crystal 500G bottles (NDC 10106-2448-1) due to subpotency.
FDA•MODERATEErbe Medical ERBEFLO CleverCap CO2 Tubing/Cap SetsErbe Medical is recalling ERBEFLO CleverCap CO2 tubing and cap sets due to a risk of unintended water flow and potential respiratory injury.
3 products
FDA•MODERATEPhilips Azurion Cable Hose CarrierPhilips is recalling Azurion imaging systems due to potential loosening or breakage of Cable Hose Carrier bolts and plastic parts.
FDA•Kian Pee Wan Dietary Supplement CapsulesKian Pee Wan dietary supplement capsules are being recalled for being marketed as an unapproved drug.
FDA•MODERATECoconut Drink 1HEYTEA USA INC is recalling Coconut Drink 1 (1L, UPC 673367992785) due to undeclared milk.
NHTSA•MODERATEAston Martin DBX Rear Lower Suspension ArmAston Martin is recalling 2021–2026 DBX models due to rear suspension arm pin failure risking loss of control.
- Equipment RecallNHTSA•MODERATETerex Pole Guide Arm Assembly Pin
Terex is recalling pole guide arm assembly pins (part 450543) due to cracked welds that may cause the arm to fall.
FDA•MODERATEDisposable Mixing Bowls with SpatulaZimmer is recalling Disposable Mixing Bowls with Spatula (Model 00-5049-011-00) due to compromised sterile barrier seals.
FDA•MODERATEBoston Scientific LUX-Dx II Arrhythmia DetectorBoston Scientific is recalling LUX-Dx II arrhythmia detectors due to a software error that prevents proper monitoring and data collection.
2 products
FDA•MODERATEVital Nutrients Aller-C CapsulesBlueroot Health is recalling Aller-C capsules due to undeclared egg, soy, and hazelnut allergens.
FDA•MODERATEPrazosin Hydrochloride Capsules 1mgAppco Pharma is recalling Prazosin Hydrochloride Capsules 1mg due to the presence of N-nitroso-prazosin impurity above acceptable limits.
3 products
NHTSA•CRITICALYamaha TW200 SpeedometerYamaha is recalling 2026 TW200 motorcycles with speedometer failure that may increase crash risk.
NHTSA•MODERATELuxfer Gas Cylinder AdapterLuxfer is recalling gas cylinder adapters (model EP-O-350-8-U5) due to O-ring incompatibility risking hydrogen leak and fire.
NHTSA•MODERATEMercedes-Benz G580 Wheel BoltsMercedes-Benz is recalling 2025 G580 vehicles with incorrect wheel bolts that may loosen or detach.
NHTSA•MODERATEMercedes-Benz 2026 GLE/GLS Passenger Air BagMercedes-Benz is recalling 2026 GLE and GLS models over passenger air bag fabric defect that may prevent deployment.
NHTSA•MODERATEKTM 390 Duke and RC 390 Throttle Control UnitKTM is recalling 2022–2024 390 Duke and RC 390 motorcycles due to throttle control unit water ingress causing loss of power.