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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
August 29, 2025VehiclesNHTSA
Renegade 2024–2025 Suspension recall
Hazard: The lowered suspension may allow the fenders to contact and damage the rear tires, increasing the risk of a crash.
August 29, 2025VehiclesNHTSA
Fontaine 2025–2026 Service Brakes, Air recall
Hazard: Driving without a functioning anti-lock brake system may result in the trailer not braking as intended, increasing the risk of a crash.
August 29, 2025Vehicle EquipmentNHTSA
Galfab Equipment recall
Hazard: A pin failure can allow the hoist to fall, increasing the risk of injury.
August 28, 2025VehiclesNHTSA
Vinfast 2023–2025 Lane Departure recall
Hazard: A steering wheel that moves unexpectedly may increase the risk of a crash.
August 28, 2025VehiclesNHTSA
Midwest Fire 2021–2025 Equipment recall
Hazard: A hose reel that detaches can become a road hazard and increase the risk of a crash. In addition, the mounting plate can fail suddenly during hose operation, increasing the risk of injury.
August 28, 2025VehiclesNHTSA
Vermeer 2025 Structure recall
Hazard: Inadequate strength of the rear impact guards can increase the risk of injury during a crash.
August 28, 2025TiresNHTSA
Goodyear Tires recall
Hazard: A loss of tire pressure increases the risk of a crash.

August 28, 2025AppliancesCPSC
TTI Outdoor Power Equipment Recalls RYOBI Pressure Washers Due to Projectile Hazard; Risk of Serious Injury
Hazard: The pressure washer's capacitor can overheat and burst, causing parts to be forcefully ejected, posing a risk of serious injury from impact to the user or bystanders.

August 28, 2025OtherCPSC
Electric Motors for Gable and Roof Mounted Attic Fans Recalled Due to Fire Hazard; Distributed by Air Vent
Hazard: The recalled electric motor's safety cutoff may pose a risk of short circuit and fire hazard while in use.

August 28, 2025Electronics & BatteriesCPSC
Party Favors Lite-Up Torches and Laser Pointers Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Multiple Standards; Imported by MTC Trading
Hazard: The recalled lite-up torches contain button cell batteries in violation of the mandatory standard for toys and the recalled mini laser pointers contain button cell batteries in violation of the mandatory standard for consumer products because the button cell batteries can be accessed easily by children. Additionally, the laser pointers do not have the warnings required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.

August 28, 2025Electronics & BatteriesCPSC
CT-ENERGY Lithium Coin Battery Chargers Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violations of Standard for Coin Battery Products and Statute for Battery Packaging; Imported by CT New Energy Technology
Hazard: The recalled battery charger violates the mandatory standard for consumer products containing button cell or coin batteries because the charger has lithium coin batteries that can be accessed easily by children. In addition, the coin batteries provided with the battery charger are not in child-resistant packaging, and the packaging does not have the warnings as required by Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

August 28, 2025FurnitureCPSC
Lulive Recalls Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violates Mandatory Standard for Clothing Storage Units; Sold on Amazon by Lulive
Hazard: The recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazards that can result in injuries or death to children. The dressers violate the mandatory standard required by the STURDY Act.

August 28, 2025Bikes & Recreational VehiclesCPSC
DT Swiss Recalls Carbon Wheels Due to Crash Hazard
Hazard: A defect in the wheel can compromise the wheel's structural integrity, posing a crash hazard.

August 28, 2025Sports & RecreationCPSC
C.A.M.P. Recalls Nimbus Lock Carabiners Due to Risk of Serious Injury or Death from Fall
Hazard: The carabiner's automatic closing mechanism can break and prevent the gate from closing, posing a risk of serious injury or death due to falling.
August 27, 2025Medical DevicesFDA
Dynex Technologies, Inc. recalls Dynex Agility Sample Tips; Model Number: 67910; The 67910 Agility Sample Tips are an accessory/consumable used with th
Hazard: The internal label affixed to the sample tip rack is incorrectly labeled as reagent tip racks. When scanned by the Agility instrument, the tip rack is misidentified as a different tip type, rendering it incompatible with the system and preventing use which causes a delay in obtaining patient results.
August 27, 2025Medical DevicesFDA
LUMENIS, LTD. recalls OtoLase Starter Kit; UPN: AC-2003748. Indicated for a variety of surgical uses including ablation, coagulation, incis
Hazard: The potential for unsterilized product within finished product labeled as sterile.
August 27, 2025Medical DevicesFDA
Boston Scientific Neuromodulation Corporation recalls Burr Hole Cover Kit, REF: M365DB4600C0; Burr Hole Cover Spares Kit, REF: M365DB4605C0. Components of Vercise Deep Stimu
Hazard: Resistance and difficulties could occur while closing the retaining clip locking mechanism, which is part of a burr hole cover kit, which is part of a Deep Brain Stimulation (DBS) system, which may lead to procedural delay, or lead-migration-which may require additional surgery.
August 27, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Electrosurgical, Cutting and Coagulation and Accessories. Electrosurgical Generator ESG-410. Model Number: WA91307C.
Hazard: Potential for the ESG-410 Electrosurgical Generator to display an error message: "E0662 System Error", followed by either automatic single reboots of the device, or continuous reboot 'loops'.
August 27, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Electrosurgical, Cutting and Coagulation and Accessories. Electrosurgical Generator ESG-410 Surgical Energy Platform (SE
Hazard: Potential for the ESG-410 Electrosurgical Generator to display an error message: "E0662 System Error", followed by either automatic single reboots of the device, or continuous reboot 'loops'.
August 27, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls Clearview Strep A Exact II Dipstick Respiratory Kit, CLIA Waived. Catalog Number: 4581225020
Hazard: Due to a classification error in the inventory management system, specific medical devices were shipped to customers that did not have the requisite license to purchase such devices.
August 27, 2025Medical DevicesFDA
Immunotech A.S. recalls Estrone RIA Catalog Number DSL8700 UDI Code: 15099590211615 Estrone RIA is an in vitro diagnostic manual medical dev
Hazard: Estrone RIA kit lots may rarely give falsely high patient results which might cause Temporary injury of Remote probability or rarely give falsely low patient results which might cause Permanent injury of Remote probability. Only in some (very rare) cases may the issue occur.
August 27, 2025Medical DevicesFDA
Ortho-Clinical Diagnostics, Inc. recalls VITROS Chemistry Products Ca Slides; Catalog Number: 145 0261;
Hazard: Generations 67 and above of VITROS Ca Slides are experiencing an increased occurrence of Condition Code TH4-63J during calibration on VITROS XT 3400 and VITROS XT 7600 Systems, causing calibration failures that delay calcium test results and potentially impact patient management. The imaging reflectometer algorithm detects excessive "spikes" (imperfections) in slide images and generates the TH4-63J condition code when the threshold of 600 spikes is exceeded. Updated analysis revealed a 19-fold increase in failure rates from 0.0043% (2024 baseline) to 0.082% for Generation 67+ slides in 2025, with 100% of calibrator failures occurring at the lowest concentration level. This can result in delayed diagnosis and treatment of conditions such as hypercalcemic crisis, parathyroid disorders, and other calcium-related emergencies requiring urgent intervention.
August 27, 2025Medical DevicesFDA
Spiggle & Theis Mt Gmbh recalls Injection needle, bayonet, Luer-Lock, 1. Model no. 50-353-23, working length 25 cm, total length 31cm, nonsterile;
Hazard: Affected product show elevated cytotoxicity values. Use of affected injection needles may present a risk of intolerance reaction or allergic reaction.
August 27, 2025Medical DevicesFDA
Drs Vascular, Inc recalls Brand Name: Q-Stop Product Name: Suture Retention Device Model/Catalog Number: QS Software Version: N/A Product Descript
Hazard: XXX
August 27, 2025Medical DevicesFDA
Pentax of America Inc recalls Pentax Medical Video Processor; Model Number: EPK-i8020c;
Hazard: During endoscopic procedures using a combination of the video processor EPK-i8020c and i20c series video endoscope, the observed image can become reddish or dark. Users have observed smoke like steam and noted that the light guide at the tip is hot during use / after the endoscope is removed from the patient and may cause thermal injury to the patient s mucous membrane.
August 27, 2025Medical DevicesFDA
Hamilton Medical AG recalls Hamilton C6 REF 160021 (ESM Board PN 10144626 UDI-DI code: 76300028PN160021ZW Hamilton C6 is a ventilator intended t
Hazard: A mechanical defect on a printed circuit board (PCB) as a result of PCB separating process. This defect might cause the ventilator to either fail at startup (no patient involvement) or during the use of the device enter ambient state, resulting in an interruption of ventilation.
August 27, 2025Medical DevicesFDA
Boston Scientific Corporation recalls RELIANCE 4-FRONT, endocardial cardioversion/defibrillation and pace/sense lead, Permanent Defibrillator Electrodes; Mode
Hazard: Affected lead models may experience gradually rising LVSI measurements in association with calcification of the defibrillation lead coils. The issue may lead to early lead replacement. Most serious harm is death or need for cardiac resuscitation.
August 27, 2025Medical DevicesFDA
Boston Scientific Corporation recalls ENDOTAK RELIANCE G/SG with 4-SITE Connector, transvenous defibrillation lead, Permanent Defibrillator Electrodes; Model
Hazard: Affected lead models may experience gradually rising LVSI measurements in association with calcification of the defibrillation lead coils. The issue may lead to early lead replacement. Most serious harm is death or need for cardiac resuscitation.
August 27, 2025Medical DevicesFDA
Boston Scientific Corporation recalls ENDOTAK RELIANCE G/SG, transvenous defibrillation lead, implantable cardioverter defibrillator (non-CRT); Model Nos. 016
Hazard: Affected lead models may experience gradually rising LVSI measurements in association with calcification of the defibrillation lead coils. The issue may lead to early lead replacement. Most serious harm is death or need for cardiac resuscitation.
August 27, 2025Food & BeverageFDA
Griffith Foods Inc. recalls BISCUIT MIX, SNG 1000042143 NET WEIGHT 2.625 LBS Packed Exclusively For: Chick-fil-A, Inc. 5200 Buffington Road Atlanta,
Hazard: Undeclared eggs