stop use immediately Recalls

2,153 recalls tagged with “stop use immediately”.

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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Health & Personal Care
HIGH
FDA DEVICE

Merit Medical 10Fore Hemostasis Valve Recalled Due to Foreign Body Risk

Merit Medical Systems recalled 447 10Fore Hemostasis Valves following a manufacturing defect that may cause foreign bodies in the fluid pathway. The silicone quad ring may be deformed or damaged during use, posing serious health risks. Patients and providers should stop using the device immediately and follow recall instructions.

Merit Medical Systems
Due to
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Health & Personal Care
HIGH
FDA DRUG

Quallent Duloxetine Delayed-Release Capsules 60 mg Recall Expanded for Impurity Above FDA Interim Lm

Quallent Pharmaceuticals Health LLC recalls 1,856 bottles of Duloxetine delayed-release capsules due to CGMP deviations and an impurity above FDA interim limits. The recall is active as of August 20, 2025. Patients and providers should stop use and contact Breckenridge Pharmaceutical or a healthcare provider for guidance.

DULOXETINE
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

Zap Surgical Systems ZAP-X Radiosurgery System Recalled for 17 Units Worldwide in 2025

Zap Surgical Systems recalled 17 ZAP-X Radiosurgery System units worldwide, including US states FL, CO, NJ, NY and several countries. A software defect could cause the collimator to collide with patient shoulders or the patient table during long gantry moves after proximity errors. Clinicians and patients should stop using the device and follow recall instructions from the manufacturer.

Zap Surgical Systems
If the
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Health & Personal Care
HIGH
FDA DEVICE

Home Health US Recalled 4,661 One Step Sterile Lancets for Single Use (2025)

Home Health US recalled 4,661 One Step Sterile Lancets for Single Use sold nationwide through Amazon. The recall cites incorrect or missing Unique Device Identifier codes. Consumers should stop using the lancets immediately and follow the recall instructions from Home Health US or their healthcare provider.

Home Health US
Due to
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Recalled FENGQS F7 Pro E-bike
HIGH
CPSC

FENGQS F7 Pro Electric Bikes Recalled for Fire Hazards Sold on Amazon (2025)

FENGQS recalled F7 Pro electric bikes with batteries produced on 2024-04-21. The bikes were sold blue and marketed under the FENGQS name. The lithium-ion battery can overheat and ignite, creating a fire and burn risk. Consumers should stop using the recalled bikes immediately and contact FENGQS for a full refund.

FENGQS
The e-bikes'
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Recalled HydroTech 5/8-inch x 25-foot Expandable Burst-Proof Hose
MEDIUM
CPSC

Winston Products HydroTech 5/8-Inch Expandable Burst-Proof Hose Recall 2025

Winston Products recalled HydroTech 5/8-inch Expandable Burst-Proof Hoses sold through Home Depot and Walmart. The hoses manufactured on or before August 31, 2024 can burst and create an impact hazard and temporarily impair hearing. Consumers should stop using the hoses immediately and contact Winston Products for a full refund.

Winston Products
The recalled
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Recalled Curtis International Minifridge Model EFMIS129 - serial numbers between A2001 to A2308 – except for model numbers containing "EFMIS129-B" or "EFMIS129-C"
HIGH
CPSC

Curtis International Recalls Frigidaire Mini Fridges After Fire Hazard (2025)

Curtis International Ltd. recalled Frigidaire-brand minifridges sold nationwide after more than $700,000 in property damage was reported. Internal electrical components can short circuit and ignite the surrounding plastic housing. Consumers should stop using recalled units immediately and contact Curtis for a full refund.

Frigidaire
The minifridges'
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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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Recalled Minecraft Light-Up Slap Ruler Bracelet, Model 718508MCR - Front
HIGH
CPSC

Innovative Designs Recalls Minecraft Light-Up Slap Ruler Bracelets (2025)

Innovative Designs recalled Minecraft Light-Up Slap Ruler Bracelets sold at retailers due to a button cell battery ingestion hazard. The recall covers models 718508MCR and 718075MCR. Consumers should stop using the recalled bracelets immediately and email disposal photos to info@innovativenyc.com to receive a full refund.

Innovative Designs
The battery
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Health & Personal Care
HIGH
FDA DRUG

Cipla USA Albuterol Sulfate Inhalation Aerosol Recall Expanded for Stability Variance (2025)

Cipla USA Inc. recalls 20,352 packs of Albuterol Sulfate Inhalation Aerosol after failing stability specifications. The defective lots were distributed nationwide in the United States. The issue involves out of specification results in particle size distribution at the 12-month time point. Patients and healthcare providers should stop use and contact Cipla USA for guidance.

Cipla USA Inc.
Failed Stability
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Recalled Aiho Five-Drawer Dresser (front)
HIGH
CPSC

Aiho Five-Drawer Dresser Recalled for Tip-Over Hazard at Walmart in 2025

Aiho recalled its five-drawer dressers sold on Walmart.com after safety concerns over tip-over and entrapment hazards. The white dressers measure about 16 inches deep, 28 inches wide, and 37 inches tall. Model AP23-W is printed on the packaging. Consumers should stop using the dresser if it is not wall-anchored and contact Aiho for a full refund and disposal instructions.

Aiho
The recalled
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