514 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
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.
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.
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.
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.
Omnia Medical recalled 15 units of the TiBrid Stand Alone Intervertebral Body Fusion Device on July 15, 2024. The recall affects devices distributed nationwide across six states due to potential failure of fusion system instruments. Patients and healthcare providers must stop using the devices immediately to avoid high-risk complications.
NOXBOX recalled 1,667 Nitric Oxide Delivery Systems on July 19, 2023. The recall addresses high failure rates of the internal Sample Pump. Patients should stop using the device immediately and follow manufacturer instructions.
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