All Product Recalls

Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

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 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 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 Due to Water Resistance Issues

Sedecal recalled nine units of its SM-40HF-Batt Mobile X-ray system on June 10, 2025, due to safety concerns. The equipment is not water-resistant and improper cleaning could lead to dangerous consequences. Patients and healthcare providers must stop using the device immediately.

SEDECAL SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

SEDECAL Recalls Mobile X-ray System Due to Water Resistance Issue

SEDECAL SA recalled 268 units of the Model Number 40KWFXPLUS Mobile X-ray system on June 10, 2025. The recall addresses concerns over improper cleaning and water resistance. Healthcare providers 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 Recalls Mobile X-ray System Over Water Resistance Risks

SEDECAL SA recalled 12 units of its Mobile X-ray system on June 10, 2025, due to water resistance issues. Users must adhere to strict cleaning instructions to avoid equipment damage. 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 Mobile X-ray System Recalled Due to Cleaning Hazard

SEDECAL SA recalled six units of its Mobile X-ray system on June 10, 2025. The device is not water-resistant and improper cleaning can lead to hazards. Healthcare providers 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 Recalled Over Water Resistance Issue

SEDECAL SA recalled eight units of its Mobile X-ray system on June 10, 2025. The recall follows warnings regarding improper cleaning due to the device's lack of water resistance. Users must stop using the equipment immediately to avoid potential hazards.

SEDECAL SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal Recalls Mobile X-ray System Due to Cleaning Hazard

Sedecal recalled 24 units of its Mobile X-ray system on June 10, 2025, due to improper cleaning risks. The equipment is not water-resistant and can lead to safety issues if not cleaned according to the manual. Healthcare providers and patients must stop using the device immediately.

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 Recalls Mobile X-ray System Over Water-Resistance Issue

SEDECAL SA recalled one Mobile X-ray system on June 10, 2025, due to a lack of water resistance. Improper cleaning can lead to serious hazards. 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 Recalls Mobile X-ray System Over Water Resistance Risk

Sedecal recalled 12 units of its Mobile X-ray system on June 10, 2025. The equipment lacks water resistance and poses a high hazard if not cleaned properly. Users must follow strict cleaning protocols to avoid serious consequences.

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
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Food & Beverages
HIGH
FDA FOOD

PRIMO NO. 1 IN PRODUCE Recalls Sliced Cucumbers Due to Salmonella

PRIMO NO. 1 IN PRODUCE recalled 89 cardboard boxes of sliced cucumbers on May 20, 2025. The product is contaminated with Salmonella, posing a serious health risk. The recall affects consumers in Virginia, New York, Pennsylvania, and New Jersey.

PRIMO NO. 1 IN PRODUCE
Product contaminated
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Food & Beverages
HIGH
FDA FOOD

PRIMO NO. 1 IN PRODUCE Recalls Cucumber Slices Due to Salmonella

PRIMO NO. 1 IN PRODUCE recalled 89 cardboard boxes of Cucumber Peeled Sliced on May 20, 2025. The product may be contaminated with Salmonella, posing a high health risk. Consumers should not consume the product and seek a refund or replacement immediately.

PRIMO NO. 1 IN PRODUCE
Product contaminated
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Food & Beverages
HIGH
FDA FOOD

PRIMO NO. 1 IN PRODUCE Recalls Vegetable Tray Cucumbers Over Salmonella Risk

PRIMO NO. 1 IN PRODUCE recalled 89 cardboard boxes of Vegetable Tray Cucumbers on May 20, 2025. The recall follows contamination with Salmonella, posing a high health risk. The affected products were distributed in Virginia, New York, Pennsylvania, and New Jersey.

PRIMO NO. 1 IN PRODUCE
Product contaminated
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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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