1,732 product recalls found in this category. Browse through all safety alerts and stay informed.
High Activity Category
This category has a significant number of recalls. Please check regularly for updates.
SEDECAL SA recalled 14 units of its SM-40HF-B-D-C mobile X-ray system on June 10, 2025. The company warned that the device is not water-resistant and improper cleaning can lead to serious consequences. Health care providers must stop using the equipment immediately and follow recall instructions.
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 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 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 one unit of its Mobile X-ray system on June 10, 2025. The device is not water-resistant and requires strict cleaning per the manual. Improper cleaning may lead to serious safety risks for patients and healthcare providers.
SEDECAL SA recalled one Mobile X-ray system on June 10, 2025, after warning that improper cleaning could lead to equipment failure. The device is not water-resistant and must be cleaned according to strict manual instructions. The recall affects units distributed in California, Illinois, and New Jersey.
Sedecal recalled one mobile X-ray system on June 10, 2025, due to concerns about improper cleaning. The model SM-40HF-B-D-C is not water-resistant and poses risks if not cleaned according to instructions. Users must stop using the device immediately and follow recall instructions.
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 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 recalled six units of its mobile X-ray system on June 10, 2025. The equipment is not water-resistant and requires strict cleaning protocols. Improper cleaning could have serious consequences for users.
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.
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.
3M recalled 530,470 Ranger Blood/Fluid Warming High Flow Sets on April 10, 2025. The recall addresses concerns about flow rates and inlet temperatures. Healthcare providers and patients must stop using the devices immediately.
ESAOTE recalled 5 Endocavity Ultrasonic Probe E 3-12 units sold in the United States to healthcare providers in NC and TX. A potential weakness in the probe body could cause liquid to leak from the terminal part of the casing near the cable. Healthcare providers and patients should stop using the device immediately and follow manufacturer instructions.
World Perfumes recalled 3,900 bottles of Iodo Blanco Iodides First Aid Antiseptic on February 13, 2025. The recall stems from reports of broken or leaking containers. Consumers should stop using the product immediately and contact their healthcare provider for guidance.
MEDITECH recalled 148 units of its clinical calculator module on February 5, 2025 due to a malfunction that may result in data loss. Users may experience issues when entering multiple keys, causing data removal from the first field of screens or questionnaires. Medical Information Technology advises immediate cessation of use.
CorNeat Vision recalled the CorNeat EverPatch surgical matrix on October 16, 2024. The recall affects the product's labeling for prevention and management of wound dehiscence. Distribution spans across the U.S. and several countries.
Olympus Corporation of the Americas recalled 633 units of the Cystoscope Outer Sheath, Model WA22810A on September 13, 2024. The recall occurred due to potential device damage when used with a GreenLight Laser for BPH therapy. Healthcare providers and patients must stop using the device immediately and follow recall instructions.
Intuitive Surgical recalled 144 units of the da Vinci 5 Surgeon Console Column Motor Connector on August 21, 2024. Users reported a potential ergonomic lock issue that could delay or abort surgical procedures. Healthcare providers must stop using the devices immediately and follow the recall instructions.
Omnia Medical recalled 15 units of the TiBrid Stand Alone Intervertebral Body Fusion Device on July 15, 2024. The recall follows reports of failure of fusion system instruments in the field. Healthcare providers and patients must stop using the device immediately.