electrical hazard Recalls

1,120 recalls tagged with “electrical hazard”.

Health & Personal Care
HIGH
FDA DEVICE

RaySearch Laboratories Recalling Radiation Therapy Software Due to Safety Risk

RaySearch Laboratories AB recalled 22 units of its radiation therapy treatment planning system on November 28, 2025. The recall affects software versions RayStation 11B and its updates due to a high hazard risk. The software may not invalidate calculated radiation doses correctly under certain conditions, potentially impacting patient safety.

RAYSEARCH LABORATORIES AB
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

RaySearch Laboratories Recalls RayStation Software for Dose Calculation Error

RaySearch Laboratories AB recalled RayStation software on November 28, 2025, due to a dose calculation error. The issue affects models 17.0.0 and 17.0.1, posing a high hazard to patients. Healthcare providers should stop using the software immediately and follow the recall instructions.

RAYSEARCH LABORATORIES AB
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

RaySearch Laboratories Recalls RayStation Software Over Dose Calculation Error

RaySearch Laboratories recalled RayStation software on November 28, 2025, due to a potential error in calculating radiation doses. The recall affects 119 units of software versions 14.0.0, 15.0.0, and 15.1.3. Healthcare providers should stop using the software immediately to ensure patient safety.

RAYSEARCH LABORATORIES AB
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

RayStation Recalls Radiation Therapy System Over Dose Calculation Flaw

RaySearch Laboratories AB recalled its RayStation/RayPlan system on November 28, 2025. The recall affects software version RayStation 10B SP1, citing a high-risk hazard in radiation dose calculations. Affected systems may not invalidate doses as intended for certain Regions of Interest.

RAYSEARCH LABORATORIES AB
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

RaySearch Laboratories Recalls Radiation Therapy Software Over Dose Calculation Error

RaySearch Laboratories recalled its RayStation and RayPlan software on November 28, 2025. The software fails to invalidate calculated radiation doses for certain Regions of Interest, posing a high risk to patients. Healthcare providers must stop using the device and follow recall instructions immediately.

RAYSEARCH LABORATORIES AB
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

RaySearch Laboratories Recalls Radiation Therapy Software Due to High Risk

RaySearch Laboratories recalled a radiation therapy treatment planning system on November 28, 2025. The recall affects 10 units of RayStation software versions 11.0.0, 11.0.1, 11.0.3, and 11.0.4. The system may inaccurately calculate radiation doses for certain Regions of Interest, posing a high risk to patients.

RAYSEARCH LABORATORIES AB
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Baxter Healthcare Recalls SIGMA Spectrum Infusion Pump Over Infusion Risk

Baxter Healthcare recalled 585 SIGMA Spectrum Infusion Pumps on November 28, 2025, due to a defect that may cause over-infusion. The affected model is the 35700BAX2, which has been distributed nationwide. Users must stop using the device immediately and follow recall instructions.

Baxter Healthcare
Certain pumps
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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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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 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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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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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 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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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 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 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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Tag Statistics

Total Recalls
1,120

Related Tags

immediate actionstop use immediatelyreturn for refundcpsc regulatedburn riskadult productfda regulatedfire hazardbathroomelectronicreplacement availablegarage