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.
2,775 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
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 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 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 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 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 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 recalled its Mobile X-ray system on June 10, 2025, due to a water resistance hazard. The company alerted users to strictly follow cleaning instructions to avoid potential harm. The recall affects devices distributed in California, Illinois, and New Jersey.
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 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 recalled 17 units of its Mobile X-ray system on June 10, 2025. The equipment is not water-resistant, posing a risk if not cleaned per manual instructions. Healthcare providers must stop using the device immediately.
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 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 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 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 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 recalled six units of its mobile X-ray system on June 10, 2025. Users must stop using the device due to a risk of malfunction if not cleaned properly. The equipment is not water-resistant, which may lead to safety hazards.
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.
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.
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 recalled 89 cardboard boxes of sliced cucumbers on May 20, 2025. The product may contain Salmonella, a serious health risk. Consumers should not eat the product and seek a refund immediately.