1,716 recalls tagged with “cpsc regulated”.
SEDECAL SA recalled one unit of its Model SM-40HF-B-D-C Mobile X-ray system on June 10, 2025. The recall follows concerns that improper cleaning may lead to equipment failure. Users in California, Illinois, and New Jersey received an email warning regarding the device's lack of water resistance.
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 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 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 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 recalled one unit of its SM-40HF-B-D-C Mobile X-ray system on June 10, 2025. The device poses a high hazard as it is not water-resistant and can lead to improper cleaning issues. Users must stop using the equipment immediately and follow the recall instructions sent via email.
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 recalled 27 units of its Mobile X-ray system on June 10, 2025. The devices lack water resistance and require strict cleaning per the manual. Improper cleaning could lead to serious issues for users.
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 recalled 39 units of its Mobile X-ray system on June 10, 2025. The device is not water-resistant and may pose a hazard if improperly cleaned. Users must follow specific cleaning instructions to avoid potential risks.
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.
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.
Chefs Warehouse recalled 15 lbs. of diced cucumbers on May 20, 2025, after discovering contamination with Salmonella. The recall includes products distributed in Maryland, Delaware, and Virginia. Consumers should not eat these cucumbers and should seek a refund or replacement immediately.
Medtronic recalled 1,440 Simplera Sensors on May 7, 2025. The device cap label may not adhere properly, compromising sterility and increasing infection risk. Patients should stop using the device immediately and contact their healthcare provider for instructions.
Ventura Foods recalled 929 cases of peanut butter and grape jelly on April 30, 2025. The company found pieces of blue plastic in the product during production. Consumers should not consume this product and can seek refunds or replacements.
Ventura Foods recalled 379 cases of its peanut butter and strawberry jam duo on April 30, 2025. Pieces of blue plastic were found in the product during production. Consumers should not eat the product and should seek a refund.
Ventura Foods recalled over 17,000 cases of creamy peanut butter on April 30, 2025. The recall follows reports of foreign blue plastic found in the product. Consumers should not consume the affected products and are urged to seek refunds.