Browse through 2,234 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
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 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 recalled four units of its Mobile X-ray system on June 10, 2025, due to water-resistance issues. Improper cleaning can lead to serious safety hazards. Users must stop using the product immediately and follow recall instructions.
Sedecal recalled three Mobile X-ray systems on June 10, 2025, after warning users about improper cleaning risks. The equipment is not water-resistant and can pose dangers if not maintained according to the manual. This recall affects units distributed in California, Illinois, and New Jersey.
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 recalled 142 units of its SM-40HF-B-D-C Mobile X-ray system on June 10, 2025. The equipment is not water-resistant and requires strict cleaning protocols to prevent hazards. Improper cleaning can lead to potentially dangerous consequences for patients and healthcare providers.
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 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 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 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 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 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 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 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.
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 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.
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 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.