These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.

High Risk Recalls

3,615 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.

What to do if you own a recalled product:

  1. Stop using the product immediately
  2. Keep the product away from children
  3. Follow the remedy instructions provided
  4. Contact the manufacturer for a refund or replacement
Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls IV Administration Sets Over High Hazard Risk

Medline Industries recalled 338 IV Administration Sets on November 26, 2025. The recall stems from complaints about malfunctioning check valve components. Patients and healthcare providers must stop using these devices immediately.

Medline Industries, LP
Medline kits
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Recalled MyOnlyStyler Root Booster Hair Dryer with the power cord cut in half for disposal
HIGH
CPSC

McLee Creations Recalls MyOnlyStyler Root Booster Hair Dryers for Electrocution Risk (2025)

McLee Creations recalled the MyOnlyStyler Root Booster Hair Dryers. The recall involves units printed with MOS-22 on the back of the handle. The product is white with black bristles and measures 12 inches long by 1.75 inches wide. The manufacturer cautions the device lacks immersion protection. Consumers should unplug and stop using recalled dryers and file for a full refund through the recall web

McLee Creations
The handheld
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Recalled Ikuso Safety Gate and Tracking Label - model Door-Gen1-123
HIGH
CPSC

Ikuso Safety Gates Recalled for Entrapment Risk After Amazon Sale (2025)

Ikuso recalled its safety pressure-mounted gates after regulators found a design flaw that could let a child’s torso pass through the opening. The white steel gates are sold in two sizes and labeled with model numbers Door-Gen1-123 and Door-Gen1-159. The recall violates the mandatory standard for expansion gates and enclosures. Consumers should stop using the gates and request a full refund by U.S

Ikuso
The recalled
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Recalled Alinux Baby Lounger in Pink
HIGH
CPSC

Alinux Baby Loungers Recalled for Entrapment and Fall Hazards in 2025

Alinux recalled its baby loungers sold on Amazon by Winkids after safety concerns. The foam pad and padded bumpers with a cloth cover and a ribbon tie create openings and low sides that can trap an infant or allow a fall. Consumers should stop using the loungers and email alinuxrecall@163.com for a full refund.

Alinux
The recalled
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Recalled Vivohome Adult Portable Bed Rail - Model VH1316-WC
HIGH
CPSC

Vivohome Recalls Adult Portable Bed Rails for Entrapment Hazard in 2025

Vivohome recalled adult portable bed rails due to a risk of entrapment and asphyxiation. The recall covers models VH1316-WC and VH1316-WH. The rails measure about 36.6 inches long, 16.1 inches wide and 15.7 inches high and have a wooden or metallic top bar with a red release button that can collapse. Stop using the recalled rails and contact Vivohome for a full refund.

Vivohome
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Homecare Beds Over Fire Hazard

Medline Industries recalled 22,565 Full Electric Low Basic Homecare Beds on November 26, 2025, due to a fire risk. The recall affects beds labeled with REF MDR107003ELO following 58 reports of overheating hand control pendants. Consumers should stop using the beds and follow recall instructions immediately.

Medline Industries, LP
Medline Industries
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Recalled Ojaswi 12-Drawer Dressers in gray (front)
HIGH
CPSC

Ebern Designs Ojaswi 12-Drawer Dressers Recalled for Tip-Over Risk (2025)

Wayfair sold the Ebern Designs Ojaswi 12-Drawer Dressers from January 2025 through October 2025 for about $75. The recall covers models HD011BL-SL and HD011WH-SL. The dressers measure 39 inches by 43 inches by 12 inches and weigh about 31.7 pounds. They can tip over if not anchored to a wall, posing a risk of serious injury or death to children. Consumers should stop using the recalled dressers if

Ebern Designs
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Homecare Beds Over Fire Hazard Risk

Medline Industries recalled 373,392 homecare beds on November 26, 2025, due to a fire hazard. The hand control pendant can overheat, causing sparking or burning. The recall affects models MDR107002E and MDR107002E-4 sold in the U.S. and Canada.

Medline Industries, LP
Medline Industries
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Homecare Beds Over Fire Risk from Hand Control

Medline Industries recalled 35,694 Full Electric Lightweight Homecare Beds on November 26, 2025, due to a fire hazard. The hand control pendant may overheat under certain conditions, leading to potential fire risks. The company received 58 complaints related to sparking and burning incidents.

Medline Industries, LP
Medline Industries
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Electric Homecare Beds Due to Fire Hazard

Medline Industries recalled 138,412 electric homecare beds on November 26, 2025. Hazardous hand control pendants may overheat and pose a fire risk. The recall follows 58 reports of sparking, burning, and smoking incidents.

Medline Industries, LP
Medline Industries
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Electric Homecare Beds Due to Fire Hazard

Medline Industries recalled 15,581 electric homecare beds on November 26, 2025, due to a fire hazard. The hand control pendant may overheat, posing a risk of fire in rare cases. The recall follows 58 complaints of sparking or burning from the pendant.

Medline Industries, LP
Medline Industries
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Homecare Beds Over Fire Hazard Risk

Medline Industries recalled 13,245 homecare beds on November 26, 2025, due to a fire risk from the hand control pendant. The company received 58 reports of sparking, burning, and smoke. Patients and healthcare providers must stop using the beds immediately and follow recall instructions.

Medline Industries, LP
Medline Industries
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Health & Personal Care
HIGH
FDA DEVICE

Philips Tempus Pro Patient Monitor Recalled Over Accuracy Issues

Philips recalled 7,129 Tempus Pro Patient Monitors on November 26, 2025. The monitors may provide unvalidated measurements for Intracranial Pressure and Bladder Pressure. Incorrect readings could lead to critical clinical decisions.

Philips
Patient monitor
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter Recalls UniCel Dxl 600 Analyzers Over Restart Issue

Beckman Coulter recalled 1,272 UniCel Dxl 600 analyzers on November 26, 2025. A communication issue may prevent the devices from restarting after shutdown, delaying test results. The recall affects multiple countries worldwide.

Beckman Coulter
Beckman Coulter
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Health & Personal Care
HIGH
FDA DRUG

Winder Laboratories Recalls Morphine Sulfate Oral Solution Over Labeling Error

Winder Laboratories, LLC recalled 3,528 bottles of Morphine Sulfate Oral Solution on November 26, 2025. The labeling error misrepresented the product size, leading to potential dosing issues. Consumers should stop using the product immediately and consult their healthcare provider.

MORPHINE SULFATE
Correct Labeled
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Recalled Outdoor Master children's helmet - model OM-TD BIKE
HIGH
CPSC

Outdoor Master OM-TD BIKE and OM-KSKB Helmets Recalled for Head Injury Risk (2025)

Outdoor Master recalled two helmet models sold and imported by Outdoor Master after a risk of serious head injury. The recall covers OM-TD BIKE and OM-KSKB helmets. The recall cites noncompliance with positional stability and coverage requirements. Stop using the recalled helmets and contact Outdoor Master for a full refund.

Outdoor Master
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Cook Medical Recalls Introducer Sheaths Over Manufacturing Errors

Cook Medical recalled 7,952 Flexor Check-Flo introducers and sets on November 26, 2025. The devices may have been manufactured out of specification, potentially posing serious risks to patients. Health care providers and patients should stop using these products immediately.

Cook
Cook Medical
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