These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.

High Risk Recalls

2,168 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.

What to do if you own a recalled product:

  1. Stop using the product immediately
  2. Keep the product away from children
  3. Follow the remedy instructions provided
  4. Contact the manufacturer for a refund or replacement
HIGHFDA 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
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HIGHFDA DEVICE

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

SEDECAL SA recalled 181 units of its Mobile X-ray system on June 10, 2025. The recall warns users that the equipment is not water-resistant and requires strict cleaning protocols. Improper cleaning may lead to serious consequences for patients and healthcare providers.

SEDECAL SA
Sedecal sent
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HIGHFDA 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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HIGHFDA 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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HIGHFDA DEVICE

Sedecal Recalls Mobile X-ray System Due to Cleaning Hazard

Sedecal recalled 55 units of its Model Number 40KWFX Mobile X-ray system on June 10, 2025. The recall addresses the device's lack of water-resistance and improper cleaning risks. Users should stop using the device immediately and follow the manufacturer's instructions.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

SEDECAL Recalls Mobile X-ray System Over Cleaning Hazard

SEDECAL SA recalled its Mobile X-ray system on June 10, 2025, due to cleaning safety concerns. The device is not water-resistant and improper cleaning may lead to serious consequences. Healthcare providers and patients must stop using the device immediately and follow recall instructions.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

Sedecal Mobile X-ray System Recalled Due to Cleaning Hazard

Sedecal recalled one Mobile X-ray system on June 10, 2025, due to improper cleaning risks. The equipment is not water-resistant and can pose serious hazards if cleaned incorrectly. Users in California, Illinois, and New Jersey should stop using the device immediately.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

SEDECAL SA Recalls Mobile X-ray System Due to Water Risk

SEDECAL SA recalled 7 units of its Mobile X-ray system on June 10, 2025. The devices may pose a water hazard due to improper cleaning. Healthcare providers must stop using this device immediately and follow the recall instructions.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

SEDECAL SA Recalls Mobile X-ray System Over Cleaning Hazard

SEDECAL SA recalled 6 units of its Mobile X-ray system on June 10, 2025. The equipment is not water-resistant and improper cleaning may lead to serious risks. Patients and healthcare providers must stop using the device immediately and follow recall instructions.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

Sedecal Recalls Mobile X-ray System Over Cleaning Hazard

Sedecal recalled two units of its Mobile X-ray system on June 10, 2025. Users must stop using the device due to improper cleaning risks. The equipment is not water-resistant, posing a high hazard to patients and healthcare providers.

SEDECAL SA
Sedecal sent
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HIGHFDA 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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HIGHFDA 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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HIGHFDA 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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HIGHFDA 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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HIGHFDA FOOD

Chefs Warehouse Issues Salmonella Recall for Sliced Cucumbers

Chefs Warehouse recalled 10 pounds of sliced cucumbers on May 20, 2025, due to Salmonella contamination. The affected products were distributed in Maryland, Delaware, and Virginia. Consumers should not consume these products and seek refunds immediately.

Chefs Warehouse
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