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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
September 18, 2025VehiclesNHTSA
Volvo 2025–2026 Exterior Lighting recall
Hazard: Trailer tail lights and turn signals that do not illuminate as intended can reduce visibility to other drivers, increasing the risk of a crash.
September 18, 2025VehiclesNHTSA
Volvo 2026 Latches/Locks/Linkages recall
Hazard: A door that cannot be opened from the inside may trap occupants, increasing the risk of injury.
September 18, 2025VehiclesNHTSA
Chevrolet, Gmc, Cadillac 2021–2024 Fuel System, Diesel recall
Hazard: A fuel leak in the presence of an ignition source increases the risk of a vehicle fire.

September 18, 2025FurnitureCPSC
EnHomee Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violates Mandatory Standard for Clothing Storage Units; Sold by EnHomee Direct
Hazard: The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in serious injuries or death to children. The dressers fail to meet the mandatory standard required by the STURDY Act.

September 18, 2025Children's ProductsCPSC
LXDHSTRA Baby Loungers and Crib Bumpers Recalled Due to Risk of Serious Injury or Death from Suffocation and Fall Hazards; Violates Federal Standard for Infant Sleep Products and Federal Crib Bumper Ban; Sold on Amazon
Hazard: The recalled baby loungers violate the mandatory standard for Infant Sleep Products. The sides are too low to contain an infant. The sleeping pad is too thick, posing a suffocation hazard. The enclosed openings at the foot of the loungers are wider than allowed, posing a fall hazard and an entrapment hazard to infants. Also, the baby loungers do not have a stand, posing a fall hazard if it is used on elevated surfaces. These violations create an unsafe sleeping environment for infants and can cause death or serious injury to infants. In addition, the recalled baby loungers come with crib bumpers, which are banned by the Federal Safe Sleep for Babies Act because the padded crib bumpers can obstruct breathing, posing a risk of serious injury or death to infants from suffocation.

September 18, 2025Children's ProductsCPSC
YooxArmor Multi-Purpose Kids' Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold on Amazon by YooxArmor
Hazard: The recalled kids' helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, positional stability, labeling and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.

September 18, 2025Children's ProductsCPSC
Youbeien Crib Mobiles Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates the Mandatory Toy Standard for Batteries; Sold on Amazon by GKKBSJ
Hazard: The recalled toys violate the mandatory standard for toys containing button batteries because the compartment that holds the batteries in the remote can be accessed without the use of a common household tool. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns and death.

September 18, 2025Electronics & BatteriesCPSC
Arizer Solo II Portable Vaporizers Recalled Due to Fire and Burn Hazards; Imported by 7111495 Canada
Hazard: The internal lithium-ion battery can overheat, produce smoke, and/or eject material, posing fire and burn hazards.

September 18, 2025OtherCPSC
Wuensche USA Recalls Ambiano Cotton Candy Makers Due to Fire Hazard; Sold at ALDI
Hazard: The heating element can cause sugar to ignite, if a consumer uses the product without the included sugar receptacle, posing a fire hazard.

September 18, 2025AppliancesCPSC
IcyBreeze Cooling Recalls Portable Misting Fans Due to Fire Hazard
Hazard: The misting fan can overheat while charging and ignite, posing a fire hazard.

September 18, 2025Electronics & BatteriesCPSC
Five Below Recalls Tabletop Fire Pits Due to Risk of Serious Burn Injury from Flame Jetting and Fire Hazards
Hazard: Alcohol fuel can splash or leak out of the fire pit reservoir during use and/or ignition, causing a flash fire that can spread and create larger hotter flames that can escape the unit, presenting risk of serious burn injury from flame jetting and fire hazards.
September 17, 2025Medical DevicesFDA
Omnia Medical recalls TiBrid Stand Alone Intervertebral Body Fusion Device, TiBrid SA Angled Screwdrivers, Sizes 30 degree, 45 degree, and 60
Hazard: Failure of fusion system instruments in the field.
September 17, 2025Medical DevicesFDA
Omnia Medical recalls TiBrid Stand Alone Intervertebral Body Fusion Device, SA Angled Punch Awl, Sizes: 30 degree, 45 degree and 60 degree.
Hazard: Failure of fusion system instruments in the field.
September 17, 2025Medical DevicesFDA
Orthofix U.S. LLC recalls PILLAR SA Ti, STERILE, 37mm (W) x 28mm (D) x 18mm (H), 20-degrees, REF: 82-3713SP
Hazard: A 37 mm implant width intervertebral body fusion device has a labeling discrepancy with incorrect width of 33 mm stated on the outer label side flap and inner label side flap information box. The 37 mm width on the front labels is correct.
September 17, 2025Medical DevicesFDA
SEASPINE ORTHOPEDICS CORPORATION recalls Reef TA Inserter, Part Number: TA2-001003, part of the Reef Interbody System
Hazard: Inserter, used as part of a system with an intervertebral body fusion device, may contribute to difficulty disengaging the implant or improper implant positioning, which may may lead to prolonged surgery, intraoperative revision, and may require the use of alternate instrumentation. Devices may also have incorrect UDI-DI marking.
September 17, 2025Medical DevicesFDA
Merit Medical Systems, Inc. recalls 10Fore Hemostasis Valve Catalog Number / UDI-DI code: MAPTEN4 / 00884450821305 MAPTEN42 / 00884450832509 MAPTEN452 /
Hazard: Due to a manufacturing issue involving the silicone quad ring where the ring is deformed or otherwise damaged and may cause a foreign body in the fluid pathway.
September 17, 2025Medical DevicesFDA
Quest International, Inc. recalls Brand Name: ReQuest Measles IgM Product Name: Enzyme Linked Immunoabsorbant Assay, Rubeola IgM Model/Catalog Number: 0
Hazard: Measles IgM Test Kit lacks premarket approval or clearance.
September 17, 2025Medical DevicesFDA
Boston Scientific Corporation recalls Preventive Maintenance (PM) Kit ICEFX, Material Number (UPN) SPRPM8000
Hazard: Certain desiccant tube subassemblies were built with end caps that were not correctly tightened.
September 17, 2025Medical DevicesFDA
Boston Scientific Corporation recalls ICEfx Cryoablation System, portable helium-free desktop cryoablation unit, Material Numbers (UPN) FPRCH8000, FPRCH8000-0
Hazard: Certain desiccant tube subassemblies were built with end caps that were not correctly tightened.
September 17, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: DJO SURGICAL Product Name: FA S Altivate Reverse Glenoid Tray Model/Catalog Number: None Software Version
Hazard: Their is a potential that the reamer may kick or bind up during or immediately prior to use.
September 17, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER SLEEVE Model/Catalog Number: 804-06-310
Hazard: Their is a potential that the reamer may kick or bind up during or immediately prior to use.
September 17, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER BOSS DRILL, 6.5mm Model/Catalog Number: 8
Hazard: Their is a potential that the reamer may kick or bind up during or immediately prior to use.
September 17, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER HEAD Model/Catalog Number: 804-06-311 Pr
Hazard: Their is a potential that the reamer may kick or bind up during or immediately prior to use.
September 17, 2025Medical DevicesFDA
Quidel Corporation recalls QuickVue: Dipstick Strep A Test: 50T, REF: 20108; 25T, REF: 20125; 50T, SCN, REF: 20108SC
Hazard: Dipstick strep A test has potential for false positive results.
September 17, 2025Medical DevicesFDA
NOXBOX LTD recalls NOxBOXi Nitric Oxide Delivery System
Hazard: Replacement of the internal Sample Pump due to high failure rates.
September 17, 2025Medical DevicesFDA
Philips Medical Systems Nederland B.V. recalls IntelliSpace Cardiovascular, Software 8.0.0.4.
Hazard: Software issue that results in the display of outdated information.
September 17, 2025Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP). Material Number: 11097543.
Hazard: Potential for falsely depressed patient, quality control (QC), and/or calibration results or delayed results.
September 17, 2025Medical DevicesFDA
Waldemar Link GmbH & Co. KG (Mfg Site) recalls LinkSymphoKnee System, Tibial Component, Modular, Symmetric, Sz. 5, CoCrMo/TiNbN, cemented, Fixed. REF Number: 880-100/
Hazard: Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured with two uncoated security screws, which is incorrect.
September 17, 2025Medical DevicesFDA
CORNEAT VISION, LTD. recalls CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 6.5 mm x 100 um, SterileEO, RX o
Hazard: Retroactive; Due to complaints, labeling correction for permanent tissue-integrating surgical matrices to include prevention and management of would dehiscence.
September 17, 2025Medical DevicesFDA
Boston Scientific Corporation recalls Boston Scientific UroMax Ultra Kit, Material Numbers (UPN): 1. M0062251200, 2. M0062251210, 3. M0062251220, 4.
Hazard: The Encore 26 Inflation Device is used with balloon dilation catheters to create and monitor pressure in the balloon and to deflate the balloon. An internal investigation determined that during use, foreign material particles could migrate from affected Encore 26 Inflation Devices into a balloon dilatation catheter.