FDA•MODERATE
Vasoview Hemopro 2 Endoscopic Vessel Harvesting System
Vasoview Hemopro 2 Endoscopic Vessel Harvesting System is recalled due to an out-of-specification sterilization dose.
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FDA•MODERATEMedtronic DLP Pediatric Arterial CannulaMedtronic recalls DLP Pediatric Arterial Cannula (CFN 77010) over loose foreign material with trace blood.
2 products
FDA•MODERATEPapablic Replacement Brush HeadsPapablic is recalling replacement brush heads over a choking hazard from breakage.
2 products
NHTSA•MODERATEOrange EV Terminal Truck Frame RailsOrange EV is recalling certain e-TRIEVER, T-Series, and HUSK-e terminal trucks due to frame rails that may crack and separate.
- Vehicle RecallNHTSA•MODERATEE-One Emergency Vehicles
E-One is recalling 2025-2026 Commercial, Typhoon N, and Cyclone N emergency vehicles due to a risk of sudden loss of drive power.
NHTSA•MODERATENissan Armada, Infiniti QX56, and QX80 Certification LabelsNissan is recalling certain Armada, QX56, and QX80 vehicles with 22-inch wheels due to incorrect GAWR labels that may lead to overloading.
FDA•MODERATECleviprex Injectable EmulsionChiesi USA is recalling Cleviprex (clevidipine injectable emulsion) 50 mg/100 mL vials due to a lack of assurance of sterility.
FDA•MODERATEAmy's Organic Lentil Soup Light in SodiumAmy's is recalling 14.5 oz cans of Organic Lentil Soup Light in Sodium due to potential spoilage.
FDA•MODERATEOla-Ola Pounded GroundnutsOla-Ola Pounded Groundnuts are recalled due to undeclared peanuts, posing a risk to consumers with peanut allergies.
FDA•MODERATEBell Pharmaceuticals: Multiple Carbamide Peroxide ProductsBell Pharmaceuticals recalls carbamide peroxide 6.5% earwax removers (CVS Health, Clinere, TopCare, etc.) for subpotency.
11 products
FDA•MODERATEWY Duck Sauce PacketsW.Y. Industries is recalling 0.35 oz. packets of WY Duck Sauce due to potential metal fragment contamination.
FDA•MODERATEOrthofix MINIRAIL Standard LengthenerOrthofix recalls MINIRAIL Standard Lengthener (M101) over incorrect labeling.
8 products
FDA•MODERATERuby Quartered Artichoke HeartsRuby Quartered Artichoke Hearts are being recalled due to potential glass contamination.
NHTSA•MODERATEWinnebago Navion and View Rooftop Ventilation FanWinnebago is recalling 2027 Navion and View RVs with MaxxAir N-Series rooftop fans due to an overheating circuit board fire risk.
2 products
NHTSA•MODERATEHyundai Kona Rear Center Seat Belt BuckleHyundai is recalling 2025 Kona Electric and 2026 Kona vehicles because the rear center seat belt buckle may fail to restrain occupants.
NHTSA•MODERATEFord Explorer Roof Rail CoversFord is recalling 2016-2019 Explorer vehicles because roof rail covers may detach, creating a road hazard.
NHTSA•MODERATEFord Aviator and Explorer Second-Row SeatsFord is recalling 2020-2027 Aviator and 2020-2026 Explorer vehicles because a faulty seat switch may cause second-row seats to move unexpectedly.
- Equipment RecallNHTSA•MODERATEFord F-150 Integrated Trailer Module Accessory Kits
Ford is recalling ITRM accessory kits for 2021-2026 F-150s due to a potential loss of trailer brakes and lighting.
NHTSA•MODERATEWabash Dry Freight Truck Liftgate Deck PinsWabash is recalling 2025-2026 Dry Freight trucks because broken liftgate deck pins may cause the platform to fall, posing an injury risk.
FDA•CRITICALKHONG GUAN (HQ): 2 productsKhong Guan recalls 14.1 oz glutinous rice balls with black sesame filling due to undeclared peanuts.
2 products
FDA•MODERATEPillsbury Bread Rolls: Hard Roll Dough and Kaiser Roll DoughGeneral Mills recalls Pillsbury Bread Rolls dough (Hard and Kaiser) over possible glass contamination.
2 products
FDA•MODERATENystatin Cream USPPadagis is recalling 15 g tubes of Nystatin Cream USP due to subpotent drug results found during stability testing.
FDA•MODERATEOptima XR200amx Radiographic SystemGE HealthCare recalls Optima XR200/220/240amx systems after column replacement due to risk of arm drop and patient injury.
3 products
FDA•MODERATEFunctional Formularies: 2 productsNutricia recalls Liquid Hope and Nourish organic meal replacement formulas due to subpotent Vitamin A.
2 products
CPSC•Cuisinart Propel+ Four Burner 3-in-1 Gas GrillCuisinart is recalling the Propel+ Four Burner 3-in-1 Gas Grill (model CGG-6331) because the pizza oven glass can shatter, posing a laceration risk.
FDA•MODERATEBoston Scientific Rapid Refill Continuous Injection SystemBoston Scientific is recalling the Rapid Refill Continuous Injection System due to a risk of syringe disconnection during use.
FDA•MODERATEICU Medical Plum Duo Infusion PumpICU Medical recalls Plum Duo Infusion Pump v1.2.3 due to risk of delivering up to twice the programmed VTBI.
2 products
FDA•CRITICALOscor Impella Introducer KitOscor recalls Abiomed Impella Introducer Kit (14F) due to sheath leakage risk.
3 products
FDA•CRITICALTransvenous Pacing Electrode TrayArgon recalls Transvenous Pacing Electrode Trays due to non-sterile lidocaine ampules in kits.
6 products
FDA•CRITICALAbiomed Impella RP Flex IntroducerAbiomed recalls Impella RP Flex introducers over sheath leakage risk.
13 products
FDA•MODERATEOlympus Toomey Evacuator 30ccOlympus recalls Toomey Evacuator 30cc (Model 188) over sterilization failure risk.
4 products
NHTSA•MODERATENAPA Steering Inner Tie Rod EndsTenneco Automotive is recalling NAPA steering inner tie rod ends distributed nationwide due to a risk of steering loss.
NHTSA•MODERATEGrand Design Lineage MaxxAir Rooftop Ventilation FanGrand Design is recalling 2026-2027 Lineage RVs with MaxxAir N-Series rooftop fans due to an overheating circuit board that poses a fire risk.
2 products- Equipment RecallNHTSA•MODERATEZoox Automated Driving System Software
Zoox is recalling ADS software that may fail to detect heavy smoke, increasing the risk of a crash in low-visibility conditions.
CPSC•Insignia Gas RangesInsignia gas ranges (models NS-RGFGSS1 and NS-RGFCGS2) are recalled due to a fire hazard from knobs that can be accidentally activated.
CPSC•BBRKIN and MouTec Biometric Gun SafesBBRKIN and MouTec biometric gun safes are recalled because the locks can be opened by unauthorized users, posing a serious injury risk.
CPSC•Flaunt MagSafe Battery ChargersFlaunt is recalling MagSafe Battery Charger model E33A due to fire and burn hazards from the lithium-ion battery overheating.
CPSC•Kobalt 24V and 48V Yard Power ToolsGreenworks is recalling 20+ models of Kobalt yard power tools due to a fire hazard when charging batteries via the USB-C port.
CPSC•Moodooy Adult Portable Bed RailsMoodooy model F311 adult portable bed rails are recalled due to serious entrapment and asphyxiation hazards.
CPSC•WonderStone Infant WalkersWonderStone infant walkers are recalled due to a fall hazard; they fail to meet mandatory safety standards for doorway and step-edge stopping.
FDA•MODERATEVersius Surgeon ConsoleCMR Surgical is recalling the Versius Surgeon Console due to a cybersecurity risk involving the Secure Boot feature.
- Device RecallFDA•MODERATETMINI Miniature Robotic System Tracking Arrays
Think Surgical is recalling TMINI Femur and Tibia Tracking Arrays because a loose knob may cause surgical misalignment.
FDA•MODERATEVitek 2 AST-N447 Test KitBiomerieux is recalling Vitek 2 AST-N447 Test Kits due to potential for false resistant results caused by pouch foil fractures.
FDA•MODERATEOmniTract Surgical Retractor SystemIntegra LifeSciences is recalling the OmniTract Surgical Retractor System due to insufficient drying time instructions in the user manual.
FDA•MODERATEGSP Neonatal GALT KitThe GSP Neonatal GALT Kit is recalled due to reduced on-board stability, which may cause test failures and delays in patient results.
FDA•MODERATEFletcher CT/MR Shielded Applicator SetElekta recalls Fletcher CT/MR applicator set due to risk of IU tube tip detachment.
3 products
NHTSA•MODERATEVolvo VHD, VNL, VNR, VN, and VAH Steering KnucklesVolvo is recalling 2026 VHD, VNL, VNR, VN, and VAH trucks due to a risk of steering control loss from loose steering arm fasteners.
FDA•MODERATEPemetrexed for Injection 100mg/VialSomerset Therapeutics recalls Pemetrexed for Injection 100mg/Vial due to cGMP deviations.
4 products
FDA•MODERATEKlowen Custom Orthodontic SolutionKlowen is recalling the Custom Orthodontic Solution, model CIAS-800033, due to a defect that may cause incorrect bracket placement.
FDA•MODERATEAtellica CH Enzymatic Hemoglobin A1c AssaySiemens is recalling the Atellica CH Enzymatic Hemoglobin A1c assay (Material No. 11097536) due to potential for inaccurate patient results.