electrical hazard Recalls

1,120 recalls tagged with “electrical hazard”.

Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA Recalls Shimadzu RF.004 Mobile X-ray System in 2025

Sedecal SA is recalling the Shimadzu RF.004 Mobile X-ray System after warnings that the device is not water-resistant and must be cleaned strictly according to the manual. Hospitals in California, Illinois, and New Jersey are affected. Stop using the device and follow recall instructions.

Sedecal SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA Recalls 4 SM-40HF-B-D-C Mobile X-ray Systems in 2025

Sedecal SA recalled 4 SM-40HF-B-D-C 40KW mobile X-ray systems sold in California, Illinois and New Jersey. A notice warns the equipment is not water-resistant and must be cleaned exactly as described in the manual to avoid possible consequences of improper cleaning. Healthcare providers should stop using the device immediately and contact Sedecal SA or their provider for instructions.

Sedecal SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

SEDECAL SA Recalled Mobile X-ray System Over Cleaning Hazard (2025)

Sedecal recalled 1 Mobile X-ray system due to major safety concerns. The device is not water-resistant and improper cleaning can cause malfunctions. Healthcare providers and patients must stop using the system immediately and follow manufacturer instructions.

SEDECAL SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA SM-40HF-B-D-C Mobile X-ray System Recalled for 27 Units in 2025

Sedecal SA recalled 27 SM-40HF-B-D-C mobile X-ray systems distributed in California, Illinois and New Jersey after warning consignees the equipment is not water-resistant and must be cleaned per the manual. The notice outlines possible consequences of improper cleaning. Hospitals and providers should stop using the device immediately and follow recall instructions.

Sedecal SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal Mobile X-ray System Recall for Not Water-Resistant Design Affects 10 Units (2025)

Sedecal SA recalls 10 SM-40HF-B-D-C mobile X-ray systems distributed in California, Illinois and New Jersey. The recall stems from a warning that the equipment is not water-resistant and must be cleaned strictly according to the manual. Hospitals and providers should stop using the device immediately and contact Sedecal for instructions.

Sedecal
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA SM-40HF-B-D-C Mobile X-ray System Recalled for Cleaning Not-Water-Resistant Risk (142 US)

Sedecal SA recalled 142 SM-40HF-B-D-C 40KW mobile X-ray systems sold to consignees in California, Illinois and New Jersey. Sedecal warned the units are not water-resistant and must be cleaned exactly as the manual prescribes, outlining the consequences of improper cleaning. Hospitals and clinics should stop using the devices immediately and follow the manufacturer's recall instructions.

Sedecal
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA Recalls 17 SM_40HF_B_D_VIR3 Mobile X-ray Systems Over Water-Resistance Cleaning Risk (202

Sedecal SA recalled 17 SM_40HF_B_D_VIR3 Mobile X-ray systems distributed in California, Illinois and New Jersey after emailing consignees that the equipment is not water-resistant and must be cleaned exactly as the manual directs. The notices warn about consequences of improper cleaning. Hospitals and clinics should stop using the device and follow the recall instructions from Sedecal SA or their

Sedecal SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA Recalls 14 SM-40HF-B-D-C Mobile X-ray Systems for Cleaning Not Water-Resistant Risk (2025

Sedecal SA recalled 14 SM-40HF-B-D-C mobile X-ray systems distributed in California, Illinois and New Jersey after notifying consignees by email that the devices are not water-resistant. The company says cleaning must follow the manual strictly, warning about possible consequences of improper cleaning. Healthcare facilities and patients should stop using the devices immediately and follow the REMS

SEDECAL SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal Mobile X-ray System Recall for 1 Unit Over Water Exposure Cleaning Hazard (2025)

Sedecal SA recalls 1 unit of Model 40KWMOBILE3.899 Mobile X-ray system distributed to consignees in the United States, including California, Illinois and New Jersey. The device is not water-resistant and must be cleaned strictly according to the manual, with the notice outlining the potential consequences of improper cleaning. Healthcare providers and patients should stop using the device immediat

Sedecal
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA 40KWFXPLUS.002 Mobile X-ray System Recalled in 2025 (8 Units)

Sedecal SA recalled 8 mobile X-ray units in the United States after notifying consignees that the equipment is not water-resistant and must be cleaned strictly per the manual. The notice warns that improper cleaning could have consequences described in the manual. Healthcare providers and patients should stop using the devices immediately and contact Sedecal SA or their healthcare provider for the

Sedecal
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA Recalls 3-Unit Mobile X-ray System 40KWFXPLUS.004 Over Cleaning and Water-Resistance Conc

Sedecal SA recalled 3 units of the Mobile X-ray system 40KWFXPLUS.004 distributed in California, Illinois and New Jersey after warning users the device is not water-resistant and must be cleaned strictly per the manual. Improper cleaning could have consequences. Stop using the device and contact Sedecal SA or your healthcare provider for instructions.

Sedecal
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

SEDECAL SA Recalls 1 Unit SM-40HF-B-D-C Mobile X-ray System (2025)

SEDECAL SA recalled 1 unit SM-40HF-B-D-C 40KW 70C EN Mobile X-ray System after emailing consignees that the equipment is not water-resistant and must be cleaned per the manual. The notice outlines possible consequences of improper cleaning. Hospitals and providers should stop using the device immediately and follow the manufacturer’s recall instructions.

SEDECAL
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA Recalls 9 SM-40HF-Batt Mobile X-ray Systems (2025)

Sedecal SA is recalling 9 units of the SM-40HF-Batt 40KW analog Mobile X-ray System distributed in California, Illinois and New Jersey. The company sent an email to consignees warning the equipment is not water-resistant and must be cleaned strictly per the manual. Improper cleaning could cause system damage. Hospitals and clinics should stop using the devices immediately and contact Sedecal SA or

Sedecal SA
Sedecal sent
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Vehicles & Parts
HIGH
NHTSA

Mercedes-Benz GLE 450E 4MATIC Recall for Rearview Mirror Attachment (2025)

Mercedes-Benz USA is recalling certain 2024 GLE 350 4MATIC, 2025 GLE 450e 4MATIC, and additional models sold through its dealer network. The issue involves a multi-purpose camera and rearview mirror that may detach from the windshield. Dealers will replace the windshield and reinstall the camera and mirror at no charge.

Mercedes-Benz
A detached
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Vehicles & Parts
HIGH
NHTSA

Mazda CX-30 2025 Air Bag Software Recall for SAS Unit (7525E)

Mazda North American Operations recalls 2024-2025 Mazda3 and CX-30 vehicles after SAS units may deactivate airbags due to a low battery condition. Dealers will reprogram the SAS unit or replace it at no charge. Owner notification letters were mailed July 24, 2025.

Mazda
Air bags
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Vehicles & Parts
HIGH
NHTSA

Kia 2025 K5 Recalled for Parking Light Flicker After PDC Software Issue

Kia America recalls 2025 K5 sedans over a software error in the Power-net Domain Controller that can cause parking lights to flicker. The recall affects 2025 K5 vehicles. Dealers will update the PDC software, or owners can receive an OTA update for free. Letters notifying owners were mailed June 24, 2025. Contact Kia customer service at 1-800-333-4542. Recall SC341.

Kia
Parking lights
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Health & Personal Care
HIGH
FDA DEVICE

Steris Recalls Barco MNA Adapter Due to Configuration Error

Steris recalled 10 units of the Barco MNA with HexaVue IP Integration System on May 23, 2025. A manufacturing error used an incorrect configuration file in a limited batch of adapter components. The recall is classified as Class II and affects states including Florida and Texas.

Steris
This is
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