NHTSA•MODERATE
International HV Service Brake System
International is recalling 2026–2027 HV vehicles for delayed service brake release that increases crash risk.
Filters
Category
Agency
Severity
Date
Distributed in
All Recalls
Back to home ←
NHTSA•MODERATEBeck/Arnley Lower Control Arm and Ball Joint AssembliesTenneco is recalling Beck/Arnley lower control arm and ball joint assemblies for 2018-2025 Subaru vehicles due to a steering loss risk.
NHTSA•MODERATEBraun Chrysler Pacifica Wheelchair Restraint RetractorBraun is recalling 2023-2026 Chrysler Pacifica vehicles because the wheelchair restraint retractor may fail to lock, increasing injury risk.
FDA•CRITICALMG217 Multi-Symptom Treatment CreamMG217 Multi-Symptom Treatment Cream recalled due to Staphylococcus aureus contamination.
FDA•MODERATEOasis Tears PF Lubricant Eye DropsOasis Tears PF eye drops (NDC 42126-6400-1) recalled due to lack of assurance of sterility.
FDA•MODERATEDakota Honey: 5 CompaniesDakota Honey recalls Spreadable Spun Honey varieties over possible metal/plastic contamination.
5 products
FDA•MODERATERevolution Ascend CTGE HealthCare recalls Revolution Ascend CT over AW Server security vulnerability.
7 products
FDA•CRITICALNamic Angiographic ManifoldMedline recalls Namic Angiographic Manifolds (SKU 64038200) due to particulate in the fluid path.
14 products
FDA•MODERATEDonJoy IceMan Classic CubeDonJoy IceMan Classic Cube recalled due to broken connector interrupting cold therapy.
4 products
NHTSA•CRITICALFontaine Fusion Flatbed Trailer Main BeamsFontaine is recalling 2025–2026 Fusion flatbed trailers; main beams may crack due to hydrogen contamination during galvanization.
NHTSA•MODERATEFan-Tastic Vent Fan LidDometic is recalling Fan-Tastic Vent Fans (6 part numbers) due to missing hinge pins that may cause lids to detach in transit.
NHTSA•MODERATE2024 Fly Wing Snake 250 EFI Brake System2024 Fly Wing Snake 250 EFI motorcycles recalled for brake pads that may fail in wet conditions.
NHTSA•MODERATESpartan RV Chassis Brake LightsShyft is recalling Spartan RV Chassis vehicles because brake lights may stay on, failing to alert other drivers and increasing crash risk.
FDA•CRITICALGeorge J Howe: 6 productsGeorge J Howe recalls sunflower seed products due to undeclared cashew allergen.
6 products
FDA•MODERATEBioCera Fibers Bone Void FillerOrthorebirth recalls BioCera Fibers bone void filler (REFs ORB-0320C-KC, ORB-0310C-KC, ORB-0304C-KC, ORB-0302C-KC, ORB-0305D-KC) for out-of-spec.
2 products
FDA•MODERATEMedline Convenience KitsMedline is recalling Ancillary Pack-LF and Open Heart Anesthesia ICC-A kits due to potential issues with sterilization and packaging calibration.
58 products
NHTSA•MODERATERam 2500 Pickup Powertrain Control ModuleChrysler recalls 2023–2026 Ram 2500 pickups; powertrain software error may allow speed to exceed tire rating.
NHTSA•MODERATEJeep Cherokee Power Transfer UnitChrysler recalls 2019–2023 Jeep Cherokee over power transfer unit failure risk.
2 products
NHTSA•CRITICALGM Cadillac, Chevrolet, GMC Transfer CaseGM is recalling 2026 Cadillac, Chevrolet, and GMC 4WD/AWD vehicles and certain 2015–2020 models due to a missing transfer case component that may cause wheel lockup.
FDA•MODERATEDuloxetine Delayed-Release Capsules 60mgBreckenridge Pharmaceutical is recalling Duloxetine 60mg capsules distributed nationwide due to the presence of an impurity above FDA limits.
FDA•MODERATENaproxen Oral SuspensionAcella Pharmaceuticals is recalling Naproxen Oral Suspension, 125 mg/5mL, distributed nationwide due to lead and lithium contamination.
FDA•MODERATEBioFire Joint Infection PanelBioFire is recalling the Joint Infection (JI) Panel due to contamination that may cause false positive test results.
- Device RecallFDA•MODERATEMint Lesion Software
Mint Medical is recalling Mint Lesion software versions 3.4.0–3.9.5 due to a risk of data loss or incorrect patient information linking.
FDA•MODERATEOne Step 10A in vitro diagnostic testOne Step 10A in vitro diagnostic test recalled for lack of FDA clearance.
7 products
FDA•MODERATEBiofire Spotfire Respiratory/Sore Throat PanelBioFire is recalling the Spotfire Respiratory/Sore Throat Panel due to the risk of false negative results and control failures.
FDA•MODERATEDEX Ophthalmic Tissue ForcepsKatalyst Surgical recalls DEX Ophthalmic Tissue Forceps, model DVF4005-23, due to IFU corrective action.
12 products
NHTSA•MODERATEMicro Bird G5 and MB II School Bus Drive Belt PulleyMicro Bird recalls 2023–2026 G5 and 2024 MB II school buses; drive belt pulley may damage oil lines and cause fire risk.
NHTSA•MODERATEMicro Bird G5 Transit Bus Drive Belt PulleyMicro Bird recalls 2023–2025 G5 transit buses; drive belt pulley may damage oil lines and cause fire risk.
FDA•CRITICALJOHN B SANFILIPPO & SONS: 6 productsJohn B. Sanfilippo recalls nut mixes over Salmonella risk.
6 products
FDA•MODERATEWoodstock Organic Shelled EdamameWoodstock Organic Shelled Edamame recalled over possible metal pieces.
FDA•MODERATEOctreotide Acetate for Injectable SuspensionTeva is recalling Octreotide Acetate 30 mg injection kits due to a lack of assurance of sterility.
2 products
FDA•MODERATEEnalapril Maleate Tablets, USP 20 mgRising Pharma is recalling Enalapril Maleate 20 mg tablets (NDC 64980-688-10) due to failed impurities test.
FDA•MODERATEBD PurPrep Sterile SolutionCareFusion is recalling BD PurPrep sterile solution due to a lack of assurance of sterility and potential product contamination.
2 products
NHTSA•MODERATETesla Model 3, Model Y, Model S, Model X Rearview CameraTesla recalls Model 3, Y, S, X vehicles with delayed rearview camera image in reverse (software 2026.8.6).
NHTSA•MODERATEWinnebago Solis Liquid Propane HoseWinnebago is recalling 2026–2027 Solis RVs; LP hose may be incorrectly routed over exhaust heat shield, risking fire.
NHTSA•MODERATE2025 Utilimaster Velocity Cargo Capacity LabelShyft is recalling 2025 Utilimaster Velocity vehicles with incorrect cargo capacity labels.
FDA•CRITICALUtz Quality Foods: Zapp's and Dirty Potato ChipsUtz is recalling Zapp's and Dirty potato chips in several varieties for possible Salmonella contamination.
6 products
FSIS•MODERATERavioli Pasta with Beef SauceRana Meal Solutions alerts on ravioli pasta mislabeled as beef and burrata that may contain shrimp and lobster, undeclared allergens.
FDA•MODERATEDELFLEX Peritoneal Dialysis SolutionFresenius recalls DELFLEX dialysis solution due to potential bag leaks compromising sterility.
2 products
FDA•MODERATEDuloxetine Delayed-Release Capsules 30 mgAjanta recalls Duloxetine 30 mg capsules over nitrosamine impurity above FDA limit.
3 products
FDA•MODERATEPhysio-Control LIFEPAK DefibrillatorsPhysio-Control is recalling various LIFEPAK defibrillators serviced without proper performance inspections, potentially delaying therapy.
NHTSA•MODERATE2026 Toyota 4Runner Load Capacity Label2026 Toyota 4Runner recalled for incorrect load capacity label that may lead to improper loading.
FDA•MODERATESecond Nature Keto Crunch Smart MixSecond Nature recalls Keto Crunch Smart Mix 10 oz pouches due to undeclared cashews, pistachios, and dried cherries.
FDA•LOWBuspirone Hydrochloride TabletsUnichem is recalling 5 mg buspirone hydrochloride tablets due to subpotency, which may reduce the medication's effectiveness.
FDA•MODERATESpacelabs Ultraview SL Command ModuleSpacelabs is recalling the Ultraview SL Command Module due to a manufacturing issue with the electrical leakage tester.
2 products
FDA•MODERATEProdisc C SK Cervical Disc ImplantCentinel Spine recalls Prodisc C SK cervical disc implants due to labeling mix-up (5mm/6mm).
2 products
FDA•CRITICALCook Centimeter Sizing CatheterCook recalls Centimeter Sizing Catheter (RPN N5.0-35-100-P-10S-PIG-CSC-20) over marker band cracking risk.
3 products
FDA•MODERATEBoston Scientific LUX-DX II Arrhythmia DetectorBoston Scientific recalls LUX-DX II Arrhythmia Detector (M302) with LATITUDE DRAGON US Server (6460) over missing PVC Burden and Bradyarrhythmia monitoring.
2 products
FDA•MODERATEERBEFLO CleverCap CO2 Tubing/Cap SetsErbe Medical recalls ERBEFLO CleverCap CO2 tubing/cap sets due to risk of water aspiration and respiratory failure.
3 products- Device RecallFDA•MODERATEda Vinci Surgical System Universal Surgical Manipulator
Intuitive Surgical is recalling the USM arm sub-assembly for da Vinci X and Xi systems due to a risk of internal screw breakage.
2 products