NHTSA•MODERATE
Horton Ambulance Touchscreen Display
Halcore recalls 2025-2026 Horton ambulances over touchscreen failure that can disable emergency lights and equipment.
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FDA•MODERATEShoolin Pharma Chem: multiple drugsShoolin Pharma Chem recalls Sildenafil and Tadalafil APIs due to CGMP deviations.
5 products
FDA•MODERATEClear Eyes Maximum Itchy Eye ReliefClear Eyes Maximum Itchy Eye Relief recalled over potential sterility issues.
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•CRITICALDairyland Jalapeno PeppersDairyland is recalling jalapeno peppers over possible Salmonella contamination.
FDA•CRITICALWhole Foods: Guacamole and Salsa DipsWhole Foods recalls guacamole and salsa dips over possible Salmonella from jalapenos.
10 products
FDA•MODERATEERBECRYO 2 Cryosurgical UnitErbe USA recalls ERBECRYO 2 Cryosurgical Unit (Model 10402-000) over risk of cryoprobe rupture from CO2 leak.
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•MODERATEStraumann Bone Level Tapered ImplantStraumann recalls BLT Implant D 4.1mm RC SLActive 14mm due to possible 12mm length mismatch.
FDA•CRITICALBaxter Duo-Vent Solution SetBaxter recalls Duo-Vent Solution Set (1C8507) over air bubble risk in drip chamber and tubing.
FDA•CRITICALMorphine Sulfate Injection 2 mg/mL Prefilled SyringesFresenius Kabi recalls Morphine Sulfate 2 mg/mL syringes over a label mixup that may contain Dilaudid.
2 products
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.
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.
- Food RecallFSIS•MODERATEJalapeño-Containing Meat and Poultry Products
FSIS alert: meat and poultry products with recalled jalapeños may be contaminated with Salmonella.
FSIS•CRITICALMidamar Beef Pastrami and Corned Beef BrisketCity Foods recalls 3,215 lbs of RTE pastrami and corned beef over Listeria risk; EST. 1896.
3 products
FSIS•CRITICALCorte Argentino Raw BeefCorte Argentino recalls 29,628 lbs of raw beef imported without reinspection; affected cuts include Top Sirloin, Eye Round, and more.
5 products
FDA•MODERATEDiovan (valsartan) 160 mg TabletsNovartis recalls Diovan (valsartan) 160 mg tablets due to failed dissolution specs.
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•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- Device RecallFDA•MODERATEnavify Digital Pathology Software
Ventana recalls navify Digital Pathology v2.5 over image/metadata discrepancy in the Viewer window.
FDA•MODERATEBOBBY Balloon Guide CatheterMicroVention recalls BOBBY Balloon Guide Catheters due to increased balloon pinhole defects.
FDA•MODERATEMirabegron Extended-Release Tablets 25 mgZydus recalls Mirabegron ER 25 mg tablets over nitrosamine impurity.
FDA•MODERATENeuroguard IEP Carotid Stent SystemContego Medical recalls Neuroguard IEP carotid stent system over filter opening failure risk.