FDA•MODERATE
Red Blood Cells, Leukocytes Reduced
LifeShare distributed leukoreduced red blood cells from a malaria-endemic-area donor.
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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 ReducedHoxworth 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.
- Food RecallFSIS•MODERATEJalapeño-Containing Meat and Poultry Products
FSIS alert: meat and poultry products with recalled jalapeños may be contaminated with Salmonella.
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- 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•MODERATEOribe Serene Scalp Densifying ShampooOribe Serene Scalp Densifying Shampoo recalled over microbial contamination.
FDA•MODERATENeuroguard IEP Carotid Stent SystemContego Medical recalls Neuroguard IEP carotid stent system over filter opening failure risk.
FDA•MODERATECOAPTIUM ConnectTISSIUM recalls COAPTIUM Connect nerve repair device over unsubstantiated 36-month shelf life.
8 products
FDA•MODERATEBlom-Singer Classic Indwelling Voice ProsthesisBlom-Singer Classic Voice Prosthesis recalled due to incorrect labeling of flange types.
2 products
FDA•MODERATEGEM Premier 7000 with iQM3Instrumentation Laboratory recalls GEM Premier 7000 with iQM3 due to lysing bag solution concentration issue.
2 products
FDA•MODERATEU2 Total Knee System Femoral Offset BushingU2 Total Knee System femoral offset bushing recalled due to incorrect engraved numbering that may cause misorientation.
2 products- Equipment RecallNHTSA•MODERATEMopar Seat Belt Assemblies
Chrysler recalls Mopar rear seat belt assemblies that may twist and fail to retract, raising injury risk.
NHTSA•MODERATEDodge Hornet and Alfa Romeo Tonale Seat BeltsChrysler recalls Dodge Hornet and Alfa Romeo Tonale rear seat belts that may twist and fail to retract.
NHTSA•MODERATEMack TerraPro Steering Gearbox FastenersMack is recalling certain 2025 TerraPro trucks over steering gearbox fasteners that may loosen.
NHTSA•MODERATEJayco Eagle Auto Leveling JacksJayco recalls 2027 Eagle, Eagle SLE, and Sundance fifth wheels over auto leveling jacks lowering in transit.