895 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 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 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 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 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 SA recalled one Mobile X-ray system on June 10, 2025, due to improper cleaning instructions. The device is not water-resistant, posing a potential hazard for users. This recall serves as a reminder to follow all cleaning protocols strictly to avoid consequences.
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 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 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 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 recalled eight units of its Easy Moving Plus Mobile X-ray system on June 10, 2025. The recall follows warnings that the equipment is not water-resistant and improper cleaning can lead to serious consequences. Users must stop using the device immediately and follow the manufacturer's instructions.
SEDECAL SA recalled five units of its Mobile X-ray system on June 10, 2025. The device is not water-resistant, posing a risk if not cleaned properly. Users must follow strict cleaning guidelines to avoid serious consequences.
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 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 three Mobile X-ray systems on June 10, 2025, due to water resistance concerns. Users must strictly adhere to cleaning instructions to prevent potential hazards. The recall affects units distributed in California, Illinois, and New Jersey.
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 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 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.
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.
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