electrical hazard Recalls

1,030 recalls tagged with “electrical hazard”.

Health & Personal Care
HIGH
FDA DEVICE

Philips Recal Size 40 L12-5 Ultrasound Transducers for Labeling Life Span Recall (2026)

Philips recalled 40 L12-5 ultrasound transducers distributed nationwide in the United States after regulators flagged labeling to define the devices' useful life. The recall concerns labeling clarity rather than a device malfunction. Healthcare providers and patients should stop using the device immediately and await instructions from Philips Ultrasound, Inc or their healthcare provider.

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound L17-5 Transducer Recalled for Useful-Life Labeling (2025)

Two Philips Ultrasound L17-5 transducers distributed nationwide to hospitals are recalled. The recall targets labeling that defines the devices' useful life. Stop using the transducers and follow Philips Ultrasound's instructions. Hospitals should contact Philips Ultrasound for guidance.

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound OMNI II TEE Transducer Recall Two Units Nationwide (2025)

Philips Ultrasound recalled 2 units of the Philips OMNI II TEE Ultrasound Transducer sold nationwide through multiple retailers. The recall seeks labeling clarification to define the transducer's useful life. Healthcare facilities should stop using the devices and follow Philips recall instructions.

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DEVICE

Spacelabs Healthcare Recalls DVI Display Cables Over Safety Risk

Spacelabs Healthcare recalled 820 DVI display cables on September 5, 2025. The cables may interfere with other medical devices due to inadequate shielding. Patients and healthcare providers should stop using these cables immediately.

Spacelabs Healthcare
Due to
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Health & Personal Care
LOW
FDA DEVICE

Philips 3D6-2 Ultrasound Transducer Recalled for Labeling Clarification (17 Units, 2025)

Philips recalled 17 units of the 3D6-2 Ultrasound Transducer distributed nationwide to healthcare facilities in the United States. The recall seeks to clarify labeling defining the transducer’s useful life. Clinicians and facilities should stop using the device immediately and follow Philips recall instructions.

Philips Ultrasound
To provide
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Recalled Cordless Grease Gun and location of Serial No.
MEDIUM
CPSC

Makita Recalls Cordless Grease Guns Over Laceration Hazard

Makita U.S.A., Inc. recalled cordless grease guns and hoses on September 4, 2025. The recall affects models XPG01S1, XPG01SR1, and XPG01Z due to a laceration hazard. Consumers should stop using the products immediately and contact Makita for a free replacement.

Makita
The flexible
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Recalled AR-15 Chamber Lock Pro (Red)
HIGH
CPSC

StopBox USA Recalls AR-15 Chamber Lock Pro Due to Injury Risk

StopBox USA recalled AR-15 Chamber Lock Pro firearm locks on September 4, 2025. A manufacturing defect allows unauthorized access to firearms, posing a risk of serious injury or death. Consumers should immediately stop using the locks and contact StopBox for refunds or replacements.

StopBox USA
A manufacturing
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Health & Personal Care
HIGH
FDA DEVICE

Lutronic Recalls Electrosurgical Unit Due to Defect Risks

Lutronic recalled 7,490 units of the XERF EFFECTOR 60 electrosurgical unit on September 4, 2025. Manufacturing defects may lead to adverse events for patients. Devices manufactured between April 1, 2025, and August 20, 2025, are affected.

Lutronic
Manufacturing defects
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Health & Personal Care
HIGH
FDA DEVICE

Philips Recalls Biplane OR Table Due to Component Deterioration

Philips Medical Systems Nederland B.V. recalled five Biplane OR Tables on September 3, 2025, due to potential failure of internal components. The recall affects models 722020 and 722025, distributed worldwide. Users must stop using the affected devices immediately to avoid operational issues.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Systems may
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls OR Tables Over Motorized Movement Failure

Philips Medical Systems Nederland B.V. recalled 174 OR tables on September 3, 2025. The recall affects models 722023, 722035, and 722015 due to potential failure of motorized movements. Users must stop using these devices immediately to prevent operational issues.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Systems may
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Imaging Systems Due to Malfunction Risk

Philips Medical Systems recalled 2,114 Allura Xper FD20 imaging systems on September 3, 2025. The systems may fail due to internal component deterioration, risking loss of motorized functionality. This recall affects 791 units in the U.S. and 1,323 globally.

Philips Medical Systems
Systems may
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Imaging System Over Malfunction Risk

Philips Medical Systems Nederland B.V. recalled 75 Allura Xper FD20/20 imaging systems on September 3, 2025. The recall affects systems due to internal component deterioration, which can hinder motorized movements. All users must stop using the device immediately and follow manufacturer instructions for safe handling.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Systems may
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Operating Room Table Over Hazard

Philips Medical Systems Netherlands B.V. recalled three Allura Xper FD20/20 OR Tables on September 3, 2025. The recall addresses potential failures in internal components that could impede motorized functions. Users must stop using the device immediately and follow recall instructions.

Philips Medical Systems Netherlands B.V.
Systems may
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls X-Ray Imaging Systems Due to Hazard

Philips Medical Systems Nederland B.V. recalled 45 Allura Xper FD20/10 imaging systems on September 3, 2025. The systems may fail due to internal component deterioration, posing a high risk to users. Affected units include 11 in the U.S. and 34 internationally.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Systems may
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls X-ray Imaging Systems Due to Malfunction Risk

Philips Medical Systems Netherlands B.V. recalled 1,117 X-ray imaging systems on September 3, 2025. The recall affects product codes 722010, 722026, and 722003 due to potential internal component deterioration. This issue may render motorized movements inoperable, posing a risk to patient care.

Philips Medical Systems Netherlands B.V.
Systems may
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Operating Room Tables Due to Hazard

Philips Medical Systems Nederland B.V. recalled two operating room tables on September 3, 2025. The recall affects models 722022 and 722033 due to potential system failures. The malfunction can inhibit motorized movements, posing a risk to patients and healthcare providers.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Systems may
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Imaging Devices Due to Hazard

Philips Medical Systems recalled 286 Allura Xper FD10/10 imaging systems on September 3, 2025. The recall affects models 722011, 722027, and 722005 due to potential failure of internal components. This malfunction could inhibit motorized movements, posing risks to patient safety.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Systems may
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Imaging System Recalled for Motorized Movement Risk

Philips Medical Systems Nederland B.V. recalled 46 imaging systems on September 3, 2025. Deterioration of internal components may lead to loss of motorized movements. Healthcare providers must stop using the systems immediately and follow recall instructions.

Philips Medical Systems Nederland B.V.
Systems may
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Radiology Imaging Systems for Safety Issues

Philips Medical Systems Nederland B.V. recalled 98 radiology imaging systems on September 3, 2025. The recall stems from internal component deterioration that may hinder motorized movements. Patients and healthcare providers must stop using the devices immediately.

Philips Medical Systems Nederland B.V.
Systems may
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Imaging Systems Over Malfunction Risk

Philips Medical Systems Nederland B.V. recalled 268 Allura Xper FD20 Biplane systems on September 3, 2025. The recall affects units distributed globally due to potential failures in internal components. If malfunction occurs, motorized movements will be disabled, posing risks to operational efficiency.

Philips Medical Systems
Systems may
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Tag Statistics

Total Recalls
1,030

Related Tags

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