FDA•MODERATE
Pemetrexed for Injection 100mg/Vial
Reliance Life Sciences recalls Pemetrexed for Injection 100mg/Vial over cGMP deviations.
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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.
FDA•MODERATEMedline Convenience KitsMedline recalls convenience kits with Covidien Mon-a-Therm probes due to distribution error.
3 products
FDA•MODERATEGasco Industrial: Multiple Isopropyl Alcohol ProductsGasco recalls Isopropyl Alcohol 70% in 16 oz, 32 oz, and 1 gal sizes due to subpotency.
6 products
FDA•MODERATEFresenius 5008X Blood Tubing SetsFresenius is recalling 5008X blood tubing sets due to potential connection errors between the tubing and the 5008X CAREsystem.
FDA•MODERATEIntracept Access InstrumentsBoston Scientific is recalling Intracept Access Instruments due to a potential sterile barrier breach that could lead to severe infection.
FDA•MODERATEEnovis EMPOWR 3D Knee InsertEncore Medical is recalling the EMPOWR 3D Knee Insert (11L 14MM) due to a packaging discrepancy involving incorrect product sizes.
2 products
FDA•MODERATEMasimo Radius VSM ECG Set and NIBP CuffMasimo recalls Radius VSM ECG Sets and NIBP Cuffs over false alarms and skin irritation risks.
2 products
FDA•LOWFexofenadine Hydrochloride Tablets 180 mgOhm Laboratories is recalling 180 mg Fexofenadine Hydrochloride tablets due to failed impurities and degradation specifications.
NHTSA•MODERATEHusqvarna and GasGas Motorcycle Rear Brake CaliperKTM is recalling certain Husqvarna and GasGas motorcycles because the rear brake caliper may crack and break, reducing braking ability.
NHTSA•MODERATEPeterbilt 579 and Kenworth T680 Air Brake ValvePACCAR is recalling certain 2026-2027 Peterbilt 579 and 2027 Kenworth T680 tractors due to an incorrectly installed air brake valve.
NHTSA•MODERATEForest River Wildwood and Salem Travel TrailersForest River is recalling 2026-2027 Wildwood and Salem travel trailers due to an incorrect GVWR on the Federal Placard.
NHTSA•MODERATEToyota and Lexus Rear Axle CarrierToyota is recalling 2026 Lexus TX and Toyota Grand Highlander vehicles due to a risk of rear axle carrier breakage and loss of vehicle control.
- Vehicle RecallNHTSA•MODERATEUtilimaster Velocity Strobe Light
Shyft is recalling 2016, 2019, and 2021 Utilimaster Velocity vehicles due to a strobe light short circuit that poses a fire risk.
NHTSA•MODERATEBMW Starter MotorBMW recalls certain 2023-2026 models over starter motor fire risk.
FDA•MODERATEMethohexital Sodium 100 mg/10 mLQuVa Pharma is recalling Methohexital Sodium 100 mg/10 mL vials due to failed impurities and degradation specifications.
FDA•MODERATEMedline Remedy Specialized Silicone CreamMedline Remedy Specialized Silicone Cream is recalled due to an out-of-specification result for formaldehyde in the raw material.
FDA•MODERATEMethohexital Sodium for Injection 500 mgAvet Pharmaceuticals is recalling Methohexital Sodium for Injection 500 mg vials due to failed impurities and degradation specifications.
FDA•MODERATEAquacel Ag Surgical SP DressingConvaTec is recalling Aquacel Ag Surgical SP dressings because they were manufactured with a thickness exceeding specifications.
FDA•MODERATEOlympus Single Use Distal CoverOlympus is replacing the previous design of the MAJ-2315 Single Use Distal Cover used with the EVIS EXERA III Duodenovideoscope.
NHTSA•MODERATEBraun Chevrolet Traverse Fuel Fill LineBraun is recalling 2026 Chevrolet Traverse vehicles due to a missing braze connection in the fuel fill line that poses a fire risk.
NHTSA•MODERATEKenway Towing Light Kits and Submersible LightsHarbor Freight is recalling Kenway towing and submersible lights that may fail to illuminate, increasing the risk of a crash.
NHTSA•MODERATESubaru Crosstrek, Forester, and Ascent Certification LabelsSubaru is recalling various Crosstrek, Forester, and Ascent models due to incorrect weight rating labels that may lead to vehicle overloading.
NHTSA•MODERATEWabash Econex Refrigerated Body Side Door StepWabash is recalling 2021-2026 Econex Refrigerated Body vehicles because the side door stirrup steps may detach, posing injury and crash risks.
NHTSA•MODERATEQ'Straint Max Wheelchair RetractorPrime-Time is recalling Q'Straint Max wheelchair retractors in 2025-2026 Ford Med Transit vans that may fail to lock and secure wheelchairs.
NHTSA•MODERATEToyota Tundra Load Carrying Capacity LabelSoutheast Toyota is recalling one 2026 Tundra truck due to an incorrect load carrying capacity label that violates federal safety standards.
FDA•MODERATECinacalcet Hydrochloride Tablets 30 mgCipla recalls Cinacalcet HCl 30 mg tablets over N-nitroso impurity above safe limit.
3 products
FDA•MODERATEDextroamphetamine/Amphetamine Extended-Release CapsulesLannett is recalling 5 mg Dextroamphetamine/Amphetamine ER capsules due to a labeling mix-up where capsules contain immediate-release pellets.
FDA•MODERATEAsclemed: Multiple Lidocaine Hcl Injection ProductsAsclemed recalls Accucaine kits and Lidocaine HCl injection ampules over sterility concerns.
2 products
FDA•MODERATEA.T.S. 4000 TS Tourniquet Dual HoseZimmer Surgical recalls A.T.S. 4000 TS Tourniquet Dual Hoses over sterility breach risk.
2 products
FDA•MODERATEGore TAG Thoracic Branch Endoprosthesis Side Branch ComponentGore is recalling 30+ models of the TAG Thoracic Branch Endoprosthesis Side Branch Component due to a risk of catheter separation.
2 products
FDA•MODERATEBard Acute Drainage TraysBard recalls Acute Drainage trays due to deficient lidocaine ampoules from supplier.
20 products
FDA•MODERATESolar GI System Water PerfusionLaborie is recalling Solar GI System configurations due to moisture accumulation that may affect pressure measurement performance.
FDA•MODERATECovidien Shiley Disposable Decannulation PlugCovidien is recalling 12+ models of Shiley Disposable Decannulation Plugs due to incorrect labeling regarding DEHP content.
2 products
NHTSA•MODERATEJayco Heartland Cyclone Travel and Fifth Wheel TrailersJayco is recalling 2026 Heartland Cyclone trailers due to a missing inverter ground connection that poses fire and electrical shock risks.
NHTSA•MODERATEJayco Seismic Fifth Toy HaulersJayco is recalling 2026 Seismic fifth toy haulers due to a missing grounding connection that poses fire and electrical shock risks.
- Vehicle RecallNHTSA•MODERATEAltec Service Body Inverter AC Wiring
Altec is recalling 2022-2026 Service Body vehicles due to a wiring defect that may cause a short circuit and increase the risk of fire.
NHTSA•MODERATENissan Leaf Rear Seat Belt RetractorsNissan is recalling 2026 Leaf vehicles because rear seat belt retractors may fail to properly secure child restraint systems.
NHTSA•MODERATEWarn Wireless Remote KitsWarn is recalling wireless remote kits (part numbers 90287 and 90289) that may cause unexpected winch movement, posing an injury risk.
FDA•MODERATEGlucagon Emergency KitLupin recalls Glucagon Emergency Kits due to a stability test failure that may impair emergency use.
3 products
FDA•MODERATEGemcitabine InjectionHikma is recalling Gemcitabine Injection due to improper temperature storage.
FDA•MODERATEZeiss Intrabeam Spherical ApplicatorZeiss is recalling the 1.5 cm Intrabeam Spherical Applicator (REF 304534-6000-557) due to failure to meet manufacturing specifications.
FDA•MODERATESiemens ARTIS icono Ceiling SuspensionSiemens is recalling the ARTIS icono ceiling suspension (Model 11328100) because monitor attachment screws may loosen over time.
- Device RecallFDA•MODERATERayCare 2024A SP1 Oncology Information Systems
RaySearch recalls RayCare 2024A SP1 over beam set delivery note data loss risk.
2 products 
FDA•MODERATEAccuray Cyberknife Xchange Robotic Collimator ChangerAccuray is recalling the Xchange Robotic Collimator Changer for the Cyberknife system due to a risk of the collimator falling from its housing.
FDA•MODERATEARTIS icono biplaneSiemens recalls ARTIS icono biplane over potential loss of detector lift movement.
3 products
FDA•MODERATEAccuray Cyberknife Xchange Robotic Collimator ChangerAccuray is recalling the Cyberknife Xchange Robotic Collimator Changer due to a risk of the component falling from its housing.
FDA•MODERATECRE Pro Wireguided Dilatation BalloonBoston Scientific recalls CRE Pro Wireguided Dilatation Balloons over potential sterile pouch breach.
12 products
FDA•MODERATEIntelliCuff Portable Cuff Pressure ControllerThe IntelliCuff pressure controller may fail to maintain cuff pressure due to a system leakage error, causing the motor to run continuously.