FDA•MODERATE
Philips Brilliance CT Scanners
Philips recalls Brilliance CT scanners over possible scan trigger failure, risking patient rescan and extra radiation.
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FDA•MODERATEAMS Spinal KitAMS SPINAL KIT recalled due to supplier quality issues with included Lidocaine HCl injection.
9 products
FDA•MODERATEMedtronic EOPA Arterial Cannula 22FRMedtronic recalls EOPA 22FR arterial cannula (Model 77422) over pinhole leak risk during bypass.
6 products
NHTSA•MODERATE2026 Entegra Anthem Motorhome Certification LabelJayco recalls 2026 Entegra Anthem motorhomes over incorrect tire size on certification label.
NHTSA•MODERATEForetravel Realm Presidential Brake LightForetravel recalls 2025-2027 Realm Presidential motorcoaches over brake lights that may stay on, increasing crash risk.
- NHTSA•MODERATEJayco Motorhome Brake Light
Jayco recalls 2025-2026 motorhomes on Spartan chassis where brake lights may stay on, increasing crash risk.
NHTSA•MODERATEPeterbilt and Kenworth Power Distribution CenterPACCAR recalls 2027 Peterbilt and Kenworth vehicles over oil-contaminated power distribution center.
FDA•MODERATEDorzolamide HCl and Timolol Maleate Ophthalmic SolutionMicro Labs recalls Dorzolamide HCl/Timolol Maleate 2%/0.5% 10mL ophthalmic solution due to defective container caps.
FDA•MODERATEMycophenolate Mofetil for InjectionMylan recalls Mycophenolate Mofetil for Injection 500 mg/vial due to precipitate.
2 products
FDA•MODERATEArgon L-Cath PICC CathetersArgon recalls L-Cath PICC catheters over hub leak/crack risk.
2 products
FDA•MODERATEAMS Medical Convenience KitsWindstone Medical recalls AMS medical convenience kits due to potential endotoxin variability in included sponges.
6 products
NHTSA•MODERATEARBOC Spirit of Independence Rear Spring HangerARBOC recalls 2017-2026 Spirit of Independence buses over rear spring hanger bolts that may detach, raising crash risk.
NHTSA•MODERATEFrontrunner Transit Bus Wheelchair Restraint RetractorFrontrunner recalls 2025 transit buses over wheelchair restraint retractors that may not lock, posing injury risk.
NHTSA•MODERATEMercedes-Benz Door Lock Micro-SwitchMercedes-Benz recalls certain 2019-2026 models over door lock micro-switch corrosion that may cause rollaway.
- Vehicle RecallNHTSA•MODERATEYamaha Boat Trailer Tongue
Midwest recalls 2027 Yamaha boat trailers over tongue failure risk.
2 products 
FDA•MODERATEFresenius Kabi: Multiple Rx Only InjectionsFresenius Kabi recalls injectables due to hair particulate matter.
5 products
FDA•MODERATERohto-Mentholatum: Multiple Rohto Cooling Eye DropsRohto Cooling Eye Drops recalled over sterility concerns; multiple formulations affected.
8 products
FDA•MODERATEGlycopyrrolate Oral Solution 1 mg/5 mLPrecision Dose recalls Glycopyrrolate Oral Solution 1 mg/5 mL over an impurity.
3 products
FDA•MODERATEMedline Convenience Kits with Bard Silastic Foley CathetersMedline recalls convenience kits with Bard Silastic Foley Catheters (sizes 16, 18, 20) due to surface raw material risk.
9 products
FDA•MODERATEMiniMed Go AppMedtronic MiniMed recalls MiniMed Go App v1.0.0 and v1.1.0 over nighttime alert failure risking missed insulin doses.
FDA•MODERATEFlexible Hystero-Fiberscope KitsKarl Storz recalls hysteroscope kits with expired endoscopic seals that may compromise sterility.
FDA•MODERATESafeOp Patient InterfaceAlphatec Spine recalls SafeOp Patient Interface over software issue causing tEMG loss, system faults, and reboot prompts.
NHTSA•MODERATEForest River Pause / OG Luxury Coach MaxxAir Fan PCBForest River recalls 2026-2027 Pause/OG Luxury Coach RVs with MaxxAir N-Series fans due to PCB overheating fire risk.
2 products
NHTSA•MODERATEForest River Travel Trailer PlacardForest River recalls 2027 travel trailers over incorrect water tank capacity on placard, risking overload and crash.
NHTSA•MODERATEBMW S 1000 RR Ignition LockBMW recalls S 1000 RR motorcycles over ignition lock failure that can stall the engine.
FDA•MODERATESnapshotGLO Wound Imaging DeviceKent Imaging recalls SnapshotGLO wound imaging devices due to battery charging failure.
FDA•MODERATEPipeline Flex Embolization DeviceMicro Therapeutics recalls Pipeline Flex Embolization Devices due to incorrect labeling of implant sizes.
4 products
FDA•MODERATEHalyard Standard Line Insertion PackAVID Medical recalls Halyard Standard Line Insertion Pack (Model PVHM234-01) over silicone seal defects causing leakage.
- Device RecallFDA•MODERATEEmano Flow v2.0.0
Emano Flow v2.0.0 recalled due to audio sampling mismatch causing biased flow rate and volume estimates.
FDA•MODERATETheraSphere 360 Y-90 Management PlatformBoston Scientific recalls TheraSphere 360 Y-90 Platform due to software anomaly causing incorrect dose calculations.
FDA•MODERATEOlympus High Flow Insufflation Unit UHI-4Olympus recalls UHI-4 insufflation unit over unexpected display shutdown and air delivery loss.
NHTSA•MODERATECoach and Equipment Phoenix/Metrolite Wheelchair LiftCoach and Equipment recalls Phoenix/Metrolite buses with S-Series wheelchair lifts due to contactor failure that may prevent stopping.
NHTSA•MODERATEATC RM500 and RM700 Winch RemoteATC recalls 2026 RM500 and RM700 trailers over winch remote incompatibility that may cause unexpected movement.
2 products
NHTSA•MODERATEHeil Side Loader Garbage Truck High Voltage CabinetHeil recalls 2025-2026 side loader garbage trucks with HH Technologies ReVamp high voltage cabinets (part 372-9585) over water intrusion risk.
2 products
NHTSA•MODERATEVolkswagen Atlas Rearview CameraVolkswagen recalls 2024-2026 Atlas vehicles over rearview camera display failure.
NHTSA•MODERATEFreightliner Low Beam HeadlightsDaimler Trucks recalls 2026-2027 Freightliner models over low beam headlight software error that reduces visibility.
NHTSA•MODERATEHiab K-HiPro Crane ColumnHiab recalls K-HiPro 425 and 505 cranes due to weld fatigue that may cause column collapse.
FDA•MODERATEPeter Rabbit Organics Banana & Strawberry Fruit PureePT Organics recalls Peter Rabbit Organics Banana & Strawberry puree pouches due to possible plastic strands.
2 products
FDA•MODERATEVentriculostomy KitMedtronic is recalling the Ventriculostomy Kit due to endotoxin levels that exceed safety limits for cerebrospinal fluid contact.
FDA•MODERATEPenumbra RED 68 Reperfusion CatheterPenumbra is recalling the RED 68 Reperfusion Catheter due to a manufacturing issue that may cause the device to fracture during use.
FDA•MODERATEWilcox BOSS Xe Aiming LasersWilcox is recalling all BOSS Xe aiming lasers to implement a safety-related software enhancement.
- Device RecallFDA•MODERATE3mensio Vascular Fenestrated Workstation Software
3mensio software may report inaccurate cardiovascular measurements when analyzing specific Philips 3D echo datasets.
FDA•MODERATESilent Nite Sleep ApplianceThe Silent Nite Sleep Appliance (Model SILNT) is being recalled because it lacks required FDA clearance.
NHTSA•MODERATEEmber Overland, E-Series, Touring Series Travel TrailersEmber recalls 2027 Overland, E-Series, and Touring trailers over incorrect VIN on certification label.
NHTSA•MODERATEFord Explorer and Lincoln Aviator Driver's SeatFord recalls 2026-2027 Explorer and Aviator over driver's seat that may recline unexpectedly.
FDA•MODERATEOlympus 4K UHD LCD MonitorOlympus is recalling the 4K UHD LCD Monitor (model OEV321UH) due to a potential connector fault that may cause image loss or abnormalities.
FDA•MODERATEAVID Medical Eye Pack Convenience KitAVID Medical is recalling the Eye Pack convenience kit (Model LVEY27) due to an incorrect concentration of Betadine solution.
FDA•MODERATESeaSpine Polyaxial HeadSeaSpine is recalling the Polyaxial Head due to a manufacturing error that may cause the component to detach during surgery.
NHTSA•MODERATEFord Bronco Engine Compartment Wiring HarnessFord recalls 2021-2026 Bronco and Bronco Raptor over wiring harness short circuit fire risk.
NHTSA•MODERATEBlue Bird Vision Brake LineBlue Bird recalls 2022-2027 Vision buses over brake line damage that may cause fluid leak, fire, or crash risk.