FDA•MODERATE
Vancomycin HCl 1.5g in 250mL Sodium Chloride Injection
Fagron recalls Vancomycin HCl 1.5g/250mL injection due to sterility concern.
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FDA•MODERATEGeri-Care Artificial Tears Lubricant Eye DropsGeri-Care Artificial Tears Lubricant Eye Drops (0.5 oz, NDC 68788-7266-0) recalled due to lack of sterility assurance.
FDA•CRITICALMedline Convenience Kits with Namic RA SyringesMedline recalls convenience kits with Namic RA syringes over risk of loose connection or disconnection during use.
25 products
FDA•MODERATEARTIS pheno and ARTIS Icono Biplane X-ray SystemSiemens is recalling ARTIS pheno and ARTIS Icono X-ray systems (Models 10849000, 11327600, 11328100, 11327700) due to erroneous dose display during patient exams.
FDA•MODERATESpacelabs Multi-parameter Command Module Model 91496Spacelabs is recalling Model 91496 Multi-parameter Command Module due to circuit board issue causing inaccurate cardiac output readings.
NHTSA•MODERATECan-Am Origin Electric Motorcycle Front Brake CaliperBRP is recalling 2025 Can-Am Origin electric motorcycles for front brake caliper failure risk.
FSIS•MODERATEGreat Value Dino Shaped Chicken NuggetsFSIS retracts alert for Great Value Dino Chicken Nuggets after follow-up testing finds no lead risk.
FDA•MODERATESee Luer Cap Set MPC-130Molded Products is recalling See Luer Cap Set MPC-130 due to threaded sleeve detachment risk.
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•MODERATEFresenius Kabi: Multiple Sale NDC Number InjectionsFresenius Kabi recalls 14 lots of Sodium Chloride and Dextrose Injections due to sterility concerns.
14 products
FDA•MODERATETornier HRS Max Tuberosity Body and Trial PartsTornier is recalling shoulder system components incorrectly labeled as HRS Max parts, as they are incompatible with the HRS Max system.
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.
3 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•MODERATEMedline Anterior Hip Pack Biopsy ValveMedline is recalling Anterior Hip Packs containing Olympus biopsy valves over risk of rubber fragment detachment.
8 products
FDA•MODERATESIGNA Premier MR Scanner Magnet FittingsGE Healthcare is recalling SIGNA Premier MR scanners due to ferrous magnet fittings that could cause personnel injury during service.
FDA•MODERATEMedtronic MiniMed Insulin PumpsMedtronic MiniMed recalls all Paradigm, 600, and BLE 700 series insulin pumps over insulin delivery errors that can cause severe hypoglycemia or ketoacidosis.
14 products
FDA•MODERATEBurlington Medical Wrap ApronsBurlington Medical wrap aprons may lose shielding effectiveness over time.
13 products
FDA•MODERATEOXOID Microbact 12L Listeria Identification KitOxoid is recalling Microbact 12L Listeria Kit (MB1128A, Lot 4494873) due to risk of incorrect organism identification from ambiguous color reactions.
- Device RecallFDA•CRITICALPhilips Respironics Trilogy Evo O2 Ventilator
Philips Respironics recalls Trilogy Evo O2 ventilators (SW 1.05.15.00) over delayed obstruction alarm.
4 products 
FDA•MODERATECardinal Health Monoject Tuberculin Syringe 1 mLCardinal Health is recalling Monoject Tuberculin Syringes (Catalog 1180100777) that contain U-100 insulin syringes instead, risking dosing errors.
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•MODERATEMeclizine Hydrochloride Tablets 12.5 mgAmerican Health Packaging is recalling Meclizine Hydrochloride 12.5 mg tablets (NDC 60687-775-65 and 60687-775-11) due to failed tablet specifications.
FDA•CRITICALCentrosFLO Hemodialysis CathetersMerit Medical recalls CentrosFLO Hemodialysis Catheters over sheath introducer defect that may cause hemorrhage and other serious complications.
5 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•MODERATEPrazosin Hydrochloride Capsules 1mgAppco Pharma recalls Prazosin HCl 1mg capsules over nitrosamine impurity (NNP) above acceptable limits.
3 products
FDA•MODERATEK.C. Pharmaceuticals: Multiple Eye DropsK.C. Pharmaceuticals recalls multiple brands of sterile eye drops over sterility concerns.
15 products
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•MODERATETramadol Hydrochloride Tablets 50 mgAmneal is recalling 500-count bottles of Tramadol Hydrochloride 50 mg tablets due to an impurity found during stability testing.
FDA•MODERATECurosurf (poractant alfa) 240 mg Intratracheal SuspensionChiesi USA is recalling Curosurf 240 mg intratracheal suspension vials (NDC 10122-510-03) due to lack of sterility assurance.
FDA•MODERATESynthes VOLT Locking Screw TapSynthes recalls VOLT Locking and Cortical Screw Taps due to incorrect thread from a lot swap.
2 products
FDA•MODERATEOlympus SOLTIVE Laser SystemOlympus recalls SOLTIVE laser systems (TFL-SLS, TFL-PLS) due to power supply defect that may cause inoperability and smoke.
2 products
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.
NHTSA•MODERATETerex Pole Guide Arm Assembly PinTerex is recalling pole guide arm assembly pins (part 450543) due to cracked welds that may cause the arm to fall.
FDA•MODERATEOctreotide Acetate Injectable Suspension 20 mgTeva recalls Octreotide Acetate 20 mg vials over sterility assurance concerns.
6 products