FDA•MODERATE
OverStitch Suture Cinch
Boston Scientific recalls OverStitch Suture Cinch over deployment and suture-cutting failures.
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FDA•MODERATEProspector Popcorn: 4 productsProspector Popcorn recalls gourmet popcorn varieties over inaccurate nutrient declarations.
4 products
FDA•MODERATETD Navio Midi Speech Generating DeviceTobii Dynavox recalls TD Navio Midi speech device over battery tab damage risk.
2 products
FDA•MODERATEArrow-LOK ImplantArrowhead recalls Arrow-LOK Implants over missing gamma radiation audit, risking infection.
2 products- Device RecallFDA•MODERATEARVIS Surgical Navigation System Gen 2
Kico Knee recalls ARVIS Surgical Navigation System Gen 2 over tilted eyepiece image from sensor issue.
2 products 
FDA•MODERATEPhilips Cardiac Workstation 5000Philips recalls Cardiac Workstation 5000 over intermittent inaccurate heart-rate data.
2 products
FDA•MODERATEDentsply Sirona Capsule MixerDentsply Sirona Capsule Mixer recalled over electrical discharge risk when unplugged.
FDA•MODERATEIntersurgical One-Piece Guedel AirwayIntersurgical recalls One-Piece Guedel Airway, size 00, ISO 5.0, Blue, due to potential occlusion.
2 products- Device RecallFDA•MODERATEHamilton Microlab STAR PCT Software
Foundation Medicine recalls Hamilton Microlab STAR PCT v2.0.0 over spontaneous software closures.
FDA•MODERATEEndoFLIP 1 SystemCovidien recalls EndoFLIP 1 System due to 24-hour limit flagging products as expired.
2 products
NHTSA•MODERATEHorton Ambulance Touchscreen DisplayHalcore recalls 2025-2026 Horton ambulances over touchscreen failure that can disable emergency lights and equipment.
FDA•MODERATEGrand Central Potato Sourdough BreadGrand Central Bakery recalls Potato Sourdough Breads due to possible metal pieces.
2 products
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•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•CRITICALOma's Pride Woof Complete Canine Chicken RecipeOma's Pride recalls Woof Complete Canine Chicken Recipe frozen dog food over potential Salmonella.
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•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•CRITICALVitasia Asian Style Wok Spice MixVitasia Asian Style Wok Spice Mix recalled due to Salmonella.
FDA•MODERATESchwarzkopf Professional Osis Grip MousseHenkel recalls Schwarzkopf Osis Grip Mousse 6.76 oz cans over explosion risk from packaging leak.
FDA•CRITICALFrankie's Organic Plant-Based Puffs Vegan CheddarFrankie's Organic Plant-Based Puffs Vegan Cheddar recalled over undeclared milk allergen.
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•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.
- 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.