electrical hazard Recalls

1,046 recalls tagged with “electrical hazard”.

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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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls IV Administration Sets Due to Valve Failure Risk

Medline Industries recalled 1,725 IV Administration Sets on November 26, 2025. The recall affects multiple kits due to potential valve malfunctions. Consumers and healthcare providers must stop using these devices immediately.

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

Medline Recalls IV Administration Sets Due to Sticking Valves

Medline Industries recalled 33 units of IV Administration Sets on November 26, 2025. The recall follows customer complaints about check valve components potentially becoming stuck. This defect poses a high risk to patient safety and requires immediate action from healthcare providers.

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

Medline Recalls IV Administration Sets Over Stuck Valve Hazard

Medline Industries recalled 16 units of IV Administration Sets on November 26, 2025. Customers reported check valve components may become stuck, posing a risk during use. Healthcare providers should stop using these devices immediately and follow recall instructions.

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

Medline Recalls IV Administration Sets Due to Valve Issues

Medline Industries recalled 5,314 IV Administration Sets on November 26, 2025. The recall affects several product SKUs due to potential failure of check valve components. Patients and healthcare providers should stop using these devices immediately.

Medline Industries, LP
Medline kits
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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 DEVICE

Medline Recalls IV Administration Sets Due to Valve Issues

Medline Industries recalled 3,045 IV administration kits on November 26, 2025. The recall affects several Medline kits due to potential malfunction of check valve components. Patients and healthcare providers should stop using these devices immediately.

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

Medline Recalls IV Administration Sets Over Valve Malfunction Risk

Medline Industries recalled 96 IV administration sets on November 26, 2025, due to a defect in the check valve. The defect can cause the valves to become stuck, posing a high risk for patients. Users should stop using the products immediately and follow the recall instructions.

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

Medline Recalls IV Administration Sets Due to Valve Malfunction

Medline Industries recalled 12 IV administration kits on November 26, 2025. The kits may contain defective check valve components that can become stuck. Patients and healthcare providers should stop using these devices immediately.

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

Cook Medical Recalls Transjugular Liver Access Set Over Hazardous Manufacturing

Cook Medical recalled 23 units of its Transjugular Liver Access Sets on November 26, 2025. The recall follows concerns that products may have been manufactured out of specification, leading to potential use errors. Healthcare providers and patients should stop using the device immediately and follow recall instructions.

Cook
Cook Medical
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls IV Administration Sets Due to Valve Malfunction

Medline Industries recalled Medline Kits containing B. Braun IV Administration Sets on November 26, 2025. The recall follows customer complaints about check valve components becoming stuck. Affected kits include the AN01 Carotid Anesth Kit-LF, SKU PHS972096014B.

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

Beckman Coulter Recalls 6,457 Immunoassay Analyzers Over Restart Issues

Beckman Coulter recalled 6,457 UniCel Dxl 800 analyzers on November 26, 2025, due to potential restart failures. The defect prevents the devices from transitioning to Ready mode, delaying patient sample processing. Healthcare providers must stop using the devices immediately and follow recall instructions.

Beckman Coulter
Beckman Coulter
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls IV Administration Sets Due to Valve Issues

Medline Industries recalled 32 units of its Deluxe Pre Op Kits on November 26, 2025. The recall stems from customer complaints about check valve components potentially sticking in open or closed positions. Patients and healthcare providers must stop using these devices immediately and follow recall instructions.

Medline Industries, LP
Medline kits
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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 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

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

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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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls IV Administration Kits Over Valve Malfunction Risk

Medline Industries recalled 11,173 IV administration kits on November 26, 2025. The kits contain B. Braun IV Administration Sets and Pump Administration Sets with faulty check valves. These valves may become stuck, posing a high hazard to patients.

Medline Industries, LP
Medline kits
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Tag Statistics

Total Recalls
1,046

Related Tags

adult productbathroomelectronicimmediate actionstop use immediatelyreturn for refundreplacement availablegaragekitchenliving roomworkplaceplastic