CPSC•
OeyUoc Pool Drain Covers
Yuanxinxiang recalls OeyUoc pool drain covers over VGBA violation posing entrapment and drowning hazards.
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CPSC•Personalized Baby Bibs and Stroller BagsPeony Design recalls baby bibs and stroller bags due to choking hazard from detaching snaps.
CPSC•Sviyatp Pool Drain CoversSviyatp pool drain covers violate VGBA entrapment standards, posing drowning hazards.
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.
NHTSA•CRITICALK&N and Spectre Fuel Filter O-RingK&N recalls fuel filters with O-ring that may disintegrate, causing fuel leak and fire risk.
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•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.
- NHTSA•MODERATEBlue Bird Vision Brake Line
Blue Bird recalls 2022-2027 Vision school buses over brake line damage risk from cotter pin contact.
FDA•CRITICALCetirizine Hydrochloride Tablets 5 mgRising Pharma recalls Cetirizine HCl 5 mg tablets due to ranitidine cross-contamination.
FDA•CRITICALTaylor Farms de Mexico S. de: 21 productsTaylor Farms recalls 21 lettuce products over Cyclospora risk.
21 products
CPSC•Cat & Jack Children's SandalsCat & Jack children's sandals are recalled due to a choking hazard from detachable pearls on the footwear.
FDA•MODERATECyproheptadine Hydrochloride SyrupRising Pharma recalls Cyproheptadine HCl Syrup 2mg/5 mL due to crystallization and floating particles.
FDA•MODERATELevothyroxine Sodium Tablets 25 mcgMajor Pharmaceuticals recalls Levothyroxine 25 mcg tablets due to subpotency.
12 products
FDA•MODERATEAmlodipine and Olmesartan Medoxomil TabletsAscend Laboratories is recalling Amlodipine and Olmesartan Medoxomil Tablets (10 mg/20 mg) due to failed dissolution specifications.
FDA•LOWTrokendi XR Topiramate ER Capsules 25mgSupernus recalls Trokendi XR 25mg capsules over failed dissolution specs.
3 products
FDA•LOWAscend Laboratories: Multiple Dabigatran Etexilate CapsulesAscend recalls Dabigatran etexilate capsules (110 mg, 150 mg) over impurity test failures.
2 products
FDA•MODERATEDivalproex Sodium Delayed-Release Tablets 500 mgBionpharma recalls Divalproex Sodium 500 mg tablets due to foreign tablets/capsules.
FDA•MODERATEFerno Power F2 Powered Fastening SystemFerno is recalling the Power F2 Powered Fastening System due to a risk of the rail mechanism lodging and preventing stretcher movement.
FDA•MODERATEHotline Fluid Warming SetICU Medical is recalling Hotline Fluid Warming Sets due to a risk of leakage at the tubing-to-connector bond.