FSIS•MODERATE
Walmart Great Value Dino Shaped Chicken Nuggets — Retraction
FSIS retracts alert for Walmart Great Value Dino Nuggets (Feb 10 2027) after confirming no lead contamination.
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NHTSA•MODERATEGreenpower Nano Beast and Beast School Bus Cross View MirrorGreenpower is recalling 2020–2024 Nano Beast and 2021–2024 Beast school buses with missing Cross View Mirror warning labels, risking driver misuse and crashes.
NHTSA•MODERATEPierce Arrow XT/Enforcer/Impel/Velocity Firm-On-Ground LightPierce is recalling 2015–2026 Arrow XT/Enforcer/Impel/Velocity aerial firetrucks; firm-on-ground light may fail to deactivate when stabilizer loses ground contact.
NHTSA•MODERATEHyundai Ioniq 6, Genesis G90, Santa Fe Seat Belt AnchorsHyundai is recalling Ioniq 6, Genesis G90, and Santa Fe vehicles over detachable seat belt anchors that may fail to restrain occupants.
FDA•MODERATEClaravis (isotretinoin capsule, USP) 10 mgTeva is recalling Claravis 10 mg capsules (NDC 0555-1054-56, 0555-1054-86) due to out-of-specification Tretinoin impurity levels.
3 products
FDA•CRITICALKirkland Signature Traditional MadeleinesKirkland Signature Traditional Madeleines are recalled due to undeclared hazelnut and soy lecithin.
FDA•MODERATEDelflex Peritoneal Dialysis SolutionFresenius Medical Care is recalling Delflex Peritoneal Dialysis Solution due to potential bag leaks and a lack of sterility assurance.
2 products
FDA•MODERATEQuickVue Dipstick Strep A TestQuidel is recalling QuickVue Dipstick Strep A Test (REF 20108) due to risk of false positive results.
FDA•MODERATELVIS Intraluminal Support DeviceMicroVention recalls LVIS Intraluminal Support Devices (REF 214022-CAS, 214518-CAS, 213517-CAS) due to dimensional nonconformance risking vessel injury or thrombosis.
FDA•MODERATELiquid Blenz Soursop BittersLiquid Blenz Soursop Bitters are recalled due to potential Clostridium botulinum contamination and unauthorized health claims.
13 products
FDA•MODERATEDakota Honey Company Spreadable Spun HoneyDakota Honey Company is recalling Original Spreadable Spun Honey due to potential contamination with stainless steel or plastic foreign objects.
5 products
NHTSA•MODERATEMercedes-Benz Drive Shaft Universal JointMercedes-Benz is recalling certain 2018–2020 E-Class and Maybach models due to drive shaft universal joint breakage risk.
NHTSA•MODERATEAutocar ACX Xpeditor Winter Front CoverAutocar recalls 2025–2026 ACX Xpeditor vehicles; winter front cover may disable forward collision warning system.
NHTSA•MODERATEGraco SnugRide Turn & Slide Infant Car SeatGraco SnugRide Turn & Slide infant car seats may detach from the base in a crash, posing injury risk.
2 products
NHTSA•CRITICALIS300 Slave Cylinder Conversion Kit Adapter PlateSleepy Customs is recalling IS300 Slave Cylinder Conversion Kits; adapter plate may separate, causing loss of clutch and gear-shift function.
FDA•MODERATEDePuy Synthes Attune Revision Hinge Femoral ComponentDePuy Synthes is recalling the Attune Revision Hinge Femoral component due to a potential loss of sterility from packaging defects.
9 products
FDA•MODERATEFain's Blackberry Honey SpreadWalker Honey Co. is recalling Fain's Blackberry Honey Spread due to potential stainless steel or plastic particle contamination.
10 products
FDA•MODERATELundberg Family Farms Jasmine White RiceLundberg Family Farms is recalling 32 oz Jasmine White Rice due to potential foreign material contamination.
FDA•MODERATEGrace Medical Stapes ProsthesisGrace Medical is recalling the Titanium/Fluoroplastic Piston Stapes Prosthesis due to incorrect functional length listed on the labeling.
FDA•MODERATEReadyMeals Turkey Bacon & Cheddar Pretzel Duo SandwichReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich is recalled due to undeclared sesame.
NHTSA•MODERATEBMW K 1600 and Grand America Reverse Gear Control UnitBMW is recalling 2017–2025 K 1600 GT/GTL/B and 2018–2025 Grand America motorcycles over reverse gear control unit overheating and fire risk.
NHTSA•MODERATEChevrolet Malibu Rearview CameraGM recalls 2023–2025 Chevrolet Malibu rearview cameras that may display distorted or blank images.
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
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.