federal law violation Recalls

305 recalls tagged with “federal law violation”.

Vehicles & Parts
HIGH
NHTSA

Ford 2025 Expedition Recalled for Brake Software Issue; OTA Update Available

Ford Motor Company recalls 2025 Expedition and other models over a brake booster software fault. The Electronic Brake Booster module may fail while driving or during ADAS use, reducing power brake assist. Ford will update the module software OTA or via dealer free of charge. Owner notifications started August 22, 2025. Contact Ford at 1-866-436-7332 for details and recall 25S77.

Ford
An unexpected
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Vehicles & Parts
HIGH
NHTSA

Hyundai IONIQ 5 2025 Recall for High Voltage Battery Bus Bar Tightening Short Circuits (2025)

Hyundai Motor America recalls 2025 IONIQ 5 vehicles due to a potentially loose bus bar in the high voltage battery system. The recall covers 2025 IONIQ 5 models. Hyundai says a short circuit could cause a fire. Owners should park outside away from structures until the remedy is complete and contact Hyundai at 1-855-371-9460. The recall number is 280.

Hyundai
An electrical
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Health & Personal Care
HIGH
FDA DRUG

Ascend Laboratories Amlodipine and Olmesartan Medoxomil Recall for Low Dissolution 8,568 Bottles in

Ascend Laboratories recalls 8,568 bottles of Amlodipine and Olmesartan Medoxomil tablets due to failed dissolution specifications. The recall covers products manufactured by Alkem Laboratories in India and distributed nationwide in the USA. The defect involves low dissolution results. Stop use immediately and contact Ascend Laboratories for guidance.

Amlodipine and Olmesartan Medoxomil
Failed Dissolution
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Health & Personal Care
HIGH
FDA DEVICE

C.R. Bard Recall: SureStep Foley Tray System Lubri-Sil I.C. Complete Care Contains Incorrect Inserts

C.R. Bard Inc. recalls 4,300 SureStep Foley Tray System Lubri-Sil I.C. Complete Care infection control Foley catheter trays nationwide in the United States. The trays may contain incorrect inserts that misrepresent material composition. The mismatch could trigger infections or allergic reactions. Health care providers should stop use and follow recall instructions immediately.

C.R. Bard
Foley catheter
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Recalled SPPTTY Kids 14-inch Bicycle in Pink
HIGH
CPSC

SPPTTY Kids Bicycles Recalled for Lead Poisoning Risk (2025)

SPPTTY recalled kids bicycles sold at Walmart after lead levels exceeded the federal lead content ban in multiple components and on the black paint used on pumps. The recall urges consumers to stop using the bicycles immediately. To receive a refund, dismantle the bicycles, photograph the setup, and email the photo to lishkjie@163.com; after destruction is verified, dispose of the bike.

SPPTTY
Multiple components
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Recalled Dearlomum retractable safety gate-black
HIGH
CPSC

Dearlomum Retractable Safety Gate Recall 2025 for Entrapment Hazard (SH20.006D)

Dearlomum retractable mesh safety gates sold on Amazon by Signbaby are recalled. The gates violate federal expansion gate standards because a child's torso can fit through the base opening, creating a risk of serious injury or death from entrapment. Stop using the recalled gates immediately and contact Signbaby for a full refund; disassemble, destroy the mesh, and email a photo to regcards.team@gm

Dearlomum
The recalled
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Recalled WLIVE Fabric 15-Drawer Dresser in Rustic Brown
HIGH
CPSC

WLIVE Fabric 15-Drawer Dressers Recalled for Tip-Over Risk Sold on Amazon (2025)

WLIVE recalled its Fabric 15-Drawer Dressers sold on Amazon after reports of tip-over and entrapment hazards. The dressers can tip when not anchored to a wall, posing serious injury or death risk to children and violating the STURDY standard. Consumers should stop using unanchored dressers and contact WLIVE for a full refund.

WLIVE
The recalled
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Health & Personal Care
HIGH
FDA DRUG

Boothwyn Pharmacy Semaglutide Injection Recall for Subpotent Drug (High-Risk)

Boothwyn Pharmacy LLC issued a nationwide recall of 186 vials of Semaglutide 2.5 mg/mL injection, 0.8 mL, on July 9, 2025. The FDA enforcement report classifies the recall as Class II with a high hazard level. Consumers and healthcare providers should stop using the product immediately and follow guidance from Boothwyn Pharmacy or a healthcare provider.

Boothwyn Pharmacy
Subpotent Drug
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Health & Personal Care
HIGH
FDA DEVICE

North American Rescue JETT Medical Device Recall for Lower-Limb Occlusion Tool (2025)

North American Rescue recalled 552 units of the JETT device, used for occlusion of blood flow to the lower limbs, due to a manufacturing defect that may compromise structural integrity and performance. The recall covers multiple kits distributed worldwide, including U.S. states and several international countries. Stop using the device immediately and await recall instructions from the company or

North American Rescue
Device used
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Vehicles & Parts
HIGH
NHTSA

Honda 2025 CR-V Hybrid Recall for Fuel Hose Installation Could Cause Fire (TLS)

Honda recalls 2025 CR-V Hybrid vehicles sold through Honda dealers nationwide after finding an improperly installed fuel feed hose that may leak. The recall is identified by Honda as TLS. Dealers will replace the fuel feed hose and install a new connector cover at no charge. Owners should contact Honda at 1-888-234-2138 for service.

Honda
A fuel
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Vehicles & Parts
HIGH
NHTSA

Ford recalls 2025 Expedition air bags for passenger-side deployment risk

Ford Motor Company recalls certain 2025 Expedition and Navigator vehicles due to a passenger-side frontal air bag that may deploy with excessive force. Dealers will replace the passenger side air bags at no charge. Owner notification letters were mailed August 8, 2025.

Ford Motor Company
An air
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Vehicles & Parts
HIGH
NHTSA

GM Recalls 2024-2025 Chevrolet Blazer EV for Parking Brake Wiring Harness Issue

GM recalls 2024-2025 Chevrolet Blazer EVs due to a rear parking brake wiring harness that may corrode or become damaged. The defect can cause unintended parking brake activation or loss of function, increasing crash risk. Dealers will inspect and reroute the harness, install anti-abrasive tape, and replace damaged harnesses at no cost. Owner notices mailed October 1, 2025. Contact Chevrolet at 1-[

CHEVROLET
Unintended activation
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Vehicles & Parts
HIGH
NHTSA

Kia 2025 K5 Recalled for Parking Light Flicker After PDC Software Issue

Kia America recalls 2025 K5 sedans over a software error in the Power-net Domain Controller that can cause parking lights to flicker. The recall affects 2025 K5 vehicles. Dealers will update the PDC software, or owners can receive an OTA update for free. Letters notifying owners were mailed June 24, 2025. Contact Kia customer service at 1-800-333-4542. Recall SC341.

Kia
Parking lights
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Vehicles & Parts
HIGH
NHTSA

VOLKSWAGEN Atlas 2024-2025 Recall: 91SB Over Rear Camera Distortion

Volkswagen Group of America recalls 2024-2025 Atlas Cross Sport and Atlas vehicles for rearview camera distortion in reverse. The defect may reduce visibility behind the vehicle and increase crash risk. Dealers will update the camera control unit software free of charge. Owner letters mailed June 5, 2025. Contact VW customer service at 1-800-893-5298.

Volkswagen
A distorted
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Vehicles & Parts
HIGH
NHTSA

Chrysler RAM ProMaster Recall 2025 for Rear-View Camera Failure

Chrysler recalls 2022-2025 Ram ProMaster vans for a rear-view camera issue. A software error in the security gateway module may prevent the rearview image from displaying. Dealers will update the software free of charge, and owner letters were mailed June 12, 2025.

Chrysler
A rearview
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Tag Statistics

Total Recalls
305

Related Tags

electrical hazardvehicleelectronicimmediate actionstop use immediatelyreplacement availablenhtsa regulatedcpsc regulatedgaragemandatory standard violationfire hazardbattery powered