immediate action Recalls

2,715 recalls tagged with “immediate action”.

Health & Personal Care
HIGH
FDA DEVICE

SEDECAL Recalls Mobile X-ray System Due to Cleaning Hazard

SEDECAL SA recalled six units of its Mobile X-ray system on June 10, 2025, due to improper cleaning risks. The equipment is not water-resistant, posing a potential hazard if not maintained according to the manual. Users must stop using the device immediately and follow recall instructions.

SEDECAL SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

SEDECAL Recalls Mobile X-ray System Over Cleaning Hazard

SEDECAL SA recalled eight mobile X-ray systems on June 10, 2025. The recall follows warnings that the devices are not water-resistant and must be cleaned per the manual. Users must stop using the device immediately to avoid potential injuries.

SEDECAL SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal Recalls Mobile X-ray System Over Water Resistance Hazard

Sedecal recalled its Mobile X-ray system, model 40KWFXPLUS.889, on June 10, 2025. The device is not water-resistant and improper cleaning can lead to serious issues. One unit distributed in California, Illinois, and New Jersey is affected.

SEDECAL SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal Mobile X-Ray Systems Recalled Over Water Resistance Issues

Sedecal recalled 56 Mobile Digital Diagnostic X-Ray Systems on June 10, 2025. The recall affects the SM-40HF-B-D-KM (AeroDR X30) model due to water resistance concerns. Users must stop using the device immediately and follow cleaning instructions to avoid potential hazards.

SEDECAL SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

SEDECAL SA Mobile X-ray System Recalled Over Cleaning Hazard

SEDECAL SA recalled 10 Mobile X-ray systems on June 10, 2025, due to a hazard related to improper cleaning. The equipment lacks water resistance, posing a risk to patients and healthcare providers. Users must stop using the device immediately and follow manufacturer instructions.

SEDECAL SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

SEDECAL Recalls Mobile X-ray System Over Cleaning Safety Hazard

SEDECAL SA recalled one unit of its mobile X-ray system on June 10, 2025. The system is not water-resistant and poses a high hazard risk due to improper cleaning. Users must stop using the device immediately and follow the recall instructions.

SEDECAL SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

SEDECAL Recalls Mobile X-Ray System Over Cleaning Hazards

SEDECAL SA recalled four units of its Mobile X-ray system on June 10, 2025, due to improper cleaning risks. The manufacturer warns the equipment is not water-resistant and requires strict adherence to cleaning instructions. Users must stop using the device immediately and follow recall instructions for safety.

SEDECAL SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal Recalls Mobile X-ray System Over Water Resistance Issue

Sedecal recalled eight units of its Easy Moving Plus Mobile X-ray system on June 10, 2025. The recall follows warnings that the equipment is not water-resistant and improper cleaning can lead to serious consequences. Users must stop using the device immediately and follow the manufacturer's instructions.

SEDECAL SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

SEDECAL Mobile X-ray System Recalled Over Water Resistance Issue

SEDECAL SA recalled one unit of its Mobile X-ray system on June 10, 2025. The device is not water-resistant and requires strict cleaning per the manual. Improper cleaning may lead to serious safety risks for patients and healthcare providers.

SEDECAL SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

SEDECAL Recalls Mobile X-ray System Over Cleaning Instructions

SEDECAL SA recalled five units of its Mobile X-ray system on June 10, 2025. The device is not water-resistant, posing a risk if not cleaned properly. Users must follow strict cleaning guidelines to avoid serious consequences.

SEDECAL SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal Recalls Mobile X-ray System Over Water Resistance Issues

Sedecal recalled one mobile X-ray system on June 10, 2025, due to concerns about improper cleaning. The model SM-40HF-B-D-C is not water-resistant and poses risks if not cleaned according to instructions. Users must 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 Due to Hazardous Cleaning Risks

SEDECAL SA recalled one Mobile X-ray system on June 10, 2025, after warning that improper cleaning could lead to equipment failure. The device is not water-resistant and must be cleaned according to strict manual instructions. The recall affects units distributed in California, Illinois, and New Jersey.

SEDECAL SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

SEDECAL Recalls Mobile X-ray System Over Water Resistance Risk

SEDECAL SA recalled 22 units of its Model SM-32HF-Batt Mobile X-ray system on June 10, 2025. The recall alerts users that the equipment is not water-resistant and requires strict cleaning per the manual. Improper cleaning may lead to serious safety risks.

SEDECAL SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

SEDECAL Recalls Mobile X-ray System Due to Cleaning Risks

SEDECAL SA recalled 1,198 units of its MobileDiagnost wDR 2.2 X-ray system on June 10, 2025. The equipment is not water-resistant and may pose hazards if not cleaned according to the manual. Users must stop using the device immediately and contact the manufacturer for further instructions.

SEDECAL SA
Sedecal sent
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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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Food & Beverages
HIGH
FDA FOOD

PRIMO No. 1 in Produce Recalls Cucumbers Due to Salmonella Risk

PRIMO No. 1 in Produce recalled 89 cardboard boxes of peeled and diced cucumbers on May 20, 2025. The product may be contaminated with Salmonella, posing a serious health risk. Consumers should not eat these cucumbers and should seek a refund or replacement.

PRIMO No. 1 in Produce
Product contaminated
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