FDA•MODERATE
Clear Eyes Maximum Itchy Eye Relief
Clear Eyes Maximum Itchy Eye Relief recalled over potential sterility issues.
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FDA•MODERATERed Blood Cells, Leukocytes ReducedRed blood cell units distributed after donor tested reactive for hepatitis C antibody.
- FDA•MODERATERed Blood Cells, Leukocytes Reduced
Hoxworth recalls Red Blood Cells, Leukocytes Reduced due to malaria risk from donor travel.
FDA•MODERATEPresource KitsCardinal Health is recalling multiple Presource procedural kits due to possible endotoxin contamination.
13 products
FDA•MODERATEBD Intravascular Administration and Extension SetsBD recalls IV administration and extension sets due to possible sterilization failure.
2 products
NHTSA•MODERATEFord Explorer Engine Rod BearingFord recalls 2026 Explorer 2.3L engines over rod bearing seizure risk.
NHTSA•MODERATEChevrolet Silverado 2500 / GMC Sierra 2500 Tire Pressure LabelGM recalls 2024-2025 Silverado 2500 and Sierra 2500 with 20-inch accessory wheels over incorrect tire pressure label.
2 products
NHTSA•MODERATEJeep Grand Cherokee Windshield WipersChrysler recalls 2026 Jeep Grand Cherokee and Grand Cherokee L over wiper failure risk.
NHTSA•MODERATEDodge Durango Rear SpoilerChrysler recalls 2021-2023 Dodge Durango rear spoilers that may detach, posing a crash risk.
NHTSA•MODERATERange Rover Front Suspension KnucklesLand Rover recalls 2016-2017 Range Rovers over incorrect front suspension knuckles that may cause loss of control.
NHTSA•MODERATENissan Altima Front Passenger Air BagsNissan recalls 2025 Altima over front air bags that may not deploy due to incorrect mounting fasteners.
NHTSA•MODERATEChrysler Rearview CameraChrysler recalls certain 2026-2027 Jeep, Ram, Chrysler, and Dodge vehicles over rearview camera display failure.
FDA•MODERATEMarketside Tomato Bisque Soup KitMarketside Tomato Bisque Soup Kit recalled due to possible Listeria contamination.
- FDA•MODERATEApheresis Red Blood Cells, Leukocytes Reduced
LifeShare Blood Centers recalls apheresis red blood cells, leukocytes reduced, from a donor with incomplete eligibility screening.
FDA•MODERATERed Blood Cells, Leukocytes ReducedLifeShare distributed leukoreduced red blood cells from a malaria-endemic-area donor.
FDA•MODERATEERBECRYO 2 Cryosurgical UnitErbe USA recalls ERBECRYO 2 Cryosurgical Unit (Model 10402-000) over risk of cryoprobe rupture from CO2 leak.
FDA•MODERATEProNephro AKI (NGAL) Reagent KitBioporto recalls ProNephro AKI (NGAL) Reagent Kit over non-validated rework that could cause missed renal disease diagnosis.
FDA•MODERATEBIOFIRE Respiratory Panel 2.1BioFire recalls BIOFIRE Respiratory Panel 2.1 over increased false negatives.
NHTSA•MODERATEBMW Driveshaft ConnectionBMW recalls certain 840i, 540i, M550i, and 750e xDrive models over driveshaft damage that can cause loss of power or rollaway.
NHTSA•MODERATEBMW X3 Steering SpindleBMW is recalling certain 2024-2026 X3 vehicles over a steering spindle that may be incorrectly attached, risking loss of steering control.
NHTSA•MODERATEGrote Replacement Marker LightsMack Trucks recalls Grote replacement marker lights (PN 78513681) that may fail to illuminate, increasing crash risk.
2 products
NHTSA•MODERATEGrote Marker LightsVolvo recalls Grote marker lights (PN 78513681) that may fail to illuminate, increasing crash risk.
2 products
NHTSA•MODERATEOdyne Hybrid System BatteryOdyne recalls hybrid systems (evAPU, G2V9) with Samsung SDI cells in Webasto battery packs due to fire risk.
FDA•MODERATESchwarzkopf Professional Osis Grip MousseHenkel recalls Schwarzkopf Osis Grip Mousse 6.76 oz cans over explosion risk from packaging leak.
FDA•MODERATEStraumann Bone Level Tapered ImplantStraumann recalls BLT Implant D 4.1mm RC SLActive 14mm due to possible 12mm length mismatch.
FDA•MODERATEEndo-Model Tibial Plateau Replacement SetWaldemar Link recalls Endo-Model tibial plateau replacement sets that may contain the wrong hinge component.
FDA•MODERATEClindamycin Palmitate Hydrochloride Oral SolutionAvet recalls Clindamycin Palmitate Oral Solution 75 mg/5 mL over particles and white flakes.
FDA•MODERATEER-Spec Vaginal SpeculumOBP Medical recalls ER-Spec X-Small vaginal speculums over a sharp-edge burr risk.
- Device RecallFDA•MODERATEPhilips Azurion Interventional X-Ray System
Philips recalls Azurion x-ray systems over software issues that may delay therapy or cause complications.
- Device RecallFDA•MODERATEPhilips Azurion Interventional Fluoroscopic X-Ray System
Philips recalls Azurion X-ray systems over software issues that may cause image degradation or loss of geometry movements.
- FDA•MODERATERed Blood Cells, Leukocytes Reduced
Hoxworth Blood Center recalls Red Blood Cells, Leukocytes Reduced over malaria risk.
FDA•MODERATEGM Helix Dental ImplantStraumann recalls GM Helix dental implants over a packaging label mismatch that could cause bone compression.
FDA•MODERATEPhilips Allura Xper FDPhilips recalls Allura Xper FD x-ray systems over firmware issue causing loss of geometry movements.
FDA•MODERATEGlidesheath Slender A-KitTerumo recalls Glidesheath Slender A-Kit 6F 10cm .021GW (60-1060) due to wrong guidewire.
NHTSA•MODERATEBlue Bird Vision Transit Bus WiringBlue Bird is recalling 2023-2027 Vision Transit Buses over a 12V wire that may short and disrupt safety functions.
NHTSA•MODERATEBlue Bird Vision School Bus Wiring HarnessBlue Bird recalls Vision School Buses over 12V wiring that may short and disrupt safety functions.
NHTSA•MODERATEMarion Body Works Pumper Fire Engine Touch ScreenMarion Body Works recalls 2025 Pumper fire engines with Weldon UV800 displays that may fail, risking loss of emergency lights.
NHTSA•MODERATEThomas Built Saf-T-Liner C2 Fuel Tank CageDTNA recalls 2024-2027 Thomas Built Saf-T-Liner C2 buses over fuel tank cage incompatibility that may cause leaks and fire risk.
NHTSA•MODERATEThomas Built Saf-T-Liner C2 Fuel Tank CageDTNA recalls 2024-2027 Thomas Built Saf-T-Liner C2 buses over fuel tank cage incompatibility that may cause fuel leaks and fire risk.
FDA•MODERATEDiovan (valsartan) 160 mg TabletsNovartis recalls Diovan (valsartan) 160 mg tablets due to failed dissolution specs.
FDA•MODERATELyle Style: 2 Made In The Columbia River Gorge WashingtonsUndeclared soy allergen in Lyle Style Bloody Mary Mix.
2 products
FDA•MODERATEVodka Tomato Sauce 24 ozSHEANDRO recalls Vodka Tomato Sauce 24 oz jars for undeclared milk allergen.
FDA•MODERATESemaglutide 12.5mg Multi-Dose VialApollo Care recalls semaglutide 12.5mg vials due to particulate matter.
11 products
FDA•MODERATENeisseria meningitidis Gp C 2ml/VLRemel recalls Neisseria meningitidis Gp C 2ml/VL (R30166901) for failing to test positive within 60 seconds.
FDA•MODERATEMedline Micro-Kill Bleach Germicidal WipesMedline Micro-Kill Bleach Germicidal Wipes may lose disinfecting strength before their 12-month shelf life ends.
4 products
FDA•MODERATEApheresis Platelets, Leukocytes ReducedSuncoast Blood Bank recalls apheresis platelets from a donor with recent malaria-area travel.
FDA•MODERATEV-Loc 90 Absorbable Wuture Closure DeviceCovidien recalls V-Loc 90 wound closure devices over possible sterile barrier tears that may cause infection or prolonged surgery.
7 products
FDA•MODERATEBoston Scientific Enhance Transcarotid/Peripheral Access KitBoston Scientific recalls Enhance Transcarotid/Peripheral Access Kits over detachable depth markings.
FDA•MODERATESpacelabs Xhibit Central Station DisplayPort SplitterSpacelabs recalls Xhibit Central Station over DisplayPort splitter audio/video failures.
2 products
FDA•MODERATEGORE VIABIL Biliary EndoprosthesisGORE VIABIL biliary endoprosthesis recalled due to mislabeling of size and drainage holes.
2 products