CPSC•
EnHomee 9-Drawer Fabric Dressers
EnHomee 9-Drawer Fabric Dressers recalled for tip-over and entrapment hazards; violates STURDY Act; sold on Walmart.com.
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CPSC•OeyUoc Pool Drain CoversYuanxinxiang recalls OeyUoc pool drain covers over VGBA violation posing entrapment and drowning hazards.
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•CRITICALMIDWEST POULTRY SERVC C/O H &: 4 productsSimple Truth Cage Free eggs recalled due to possible Salmonella Enteritidis.
4 products
FSIS•CRITICALtasty KITCHEN Chicken Noodle Condensed SoupBCI Foods recalls 4,300 lbs of tasty KITCHEN Chicken Noodle Soup due to import violation.
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 Pediatric Open Heart KitMedline is recalling convenience kits containing BD PurPrep 26 mL over possible Bacillus contamination.
4 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.
FDA•MODERATEMan Fon: 2 Wonton WrappersMan Fon recalls Won Ton Wrappers Extra Thin over undeclared Yellow #5 and #6 colors.
2 products
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•CRITICALMedline Anterior Hip KitMedline is recalling anterior hip kits containing Bupivacaine Hydrochloride in Dextrose Injection over quality issues.
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.
FDA•MODERATEAXP Processing Bag SetThermoGenesis recalls AXP Processing Bag Set, Model 8-5101, over stopcock particulates in sterile fluid path.
FDA•CRITICALMedline HIP CDS-LF KitMedline is recalling specific lots of procedure kits containing Bupivacaine ampules due to a quality issue that could cause drug ineffectiveness.
4 products
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•CRITICALSpicy Breakfast BurritosM.G. Foods recalls Spicy Breakfast Burritos due to undeclared soy allergen.
FDA•CRITICALOrganic Moringa PowderGreen Jeeva is recalling bulk 15kg bags of Organic Moringa Powder (code GJ96) due to potential Salmonella contamination.
FDA•MODERATEBrooklyn Roasting Cold Brew ConcentrateBrooklyn Roasting recalls cold brew concentrate 2.5gal over possible botulism risk.
FDA•MODERATEVentriculostomy KitMedtronic is recalling the Ventriculostomy Kit due to endotoxin levels that exceed safety limits for cerebrospinal fluid contact.
FDA•LOWShandong Ling Xian Food: 6 Serve Hot Or Cold IngredientsIsland Pacific and Nautilus imitation crab sticks and flakes recalled for undeclared STTP.
6 products
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•LOWLidolog KitLidolog Kit is being recalled because the label wrap obscures the barcode, making it difficult to scan.
2 products
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.