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All product recalls affecting Kansas.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Kansas in the distribution area.
Forest River, Inc. (Forest River) is recalling certain 2025 Shasta Oasis and Spirit travel trailers equipped with InVision Three Burner Cooktops. The aluminum burner tube may crack and cause a gas leak.
Possibility of the patient falling from the table related to the mattress used on the patient table.
Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel
Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel
Potential that the induction seal is not completely sealed to the device tube packaging.
Due to manufacturing issue (unintended by-product of the injection molding process) a sharp pin that may puncture the blister packaging and breaching the sterile barrier of the finished product.
Use of Tack Endovascular system, designed to treat acute dissections of inner wall or lining of an artery by tacking damaged tissue to inner luminal surface, could result in problems with deployment and stability of device in vessel after deployment, which may cause failure to resolve dissection, migration of implant, bailout stenting, reintervention, unintended removal of tack devices, and ischemia.
Automated dispensing device labeling is being updated to strengthen labeling around manual access to medications to address the risk of potential delays in retrieving contents/ accessing medications that may result from power loss or potential automated dispensing device malfunctions.
Failed Stability Specifications - 12-month stability test result for one of the known peptides is below the specification limit
Product complaints were received describing the A820 myPTM app taking longer than expected for patients to interact with their implantable pump.
The machine side connector of the filter HME may be occluded by plastic which prevents proper airflow. The issue may lead to ventilation bag malfunction in which the user is unable to inflate/deflate properly during manual ventilation. Potential risks to health include oxygen deprivation, leading to respiratory distress and medical complications.
The machine side connector of the filter HME may be occluded by plastic which prevents proper airflow. The issue may lead to ventilation bag malfunction in which the user is unable to inflate/deflate properly during manual ventilation. Potential risks to health include oxygen deprivation, leading to respiratory distress and medical complications.
The MSOT Acuity Echo does not include an adequate instruction for safe operation of the device. The previous version of the user manuals contained a wrong value for the Nominal Ocular Hazard Distance (NOHD).
Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms.
Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms.
Labeling update to include a contraindication statement against the use of medicine cabinets in procedure and operating rooms.
Software issues could potentially result in: 1) delays in accessing dispensing software application, 2) wrong therapy (dose, item, timing, etc.), or 3) unauthorized access and/or compliance related issues
Labeling is insufficient regarding delays in access to medication. The firm is strengthening the label as an additional risk mitigation.
Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them from securely fitting into the compatible handpiece.
This recall involves SIG SAUER ROMEO5 Red Dot Sights, Models SOR52001 and 7400579, which is a part included with Model SORJ53101. They are labeled with the SIG SAUER logo and ROMEO5 name on one side of the product. The model number can be found on the product packaging. The recalled dot sights contain either the letter K or M as the last digit of the serial number printed on the bottom of the sight. Sig Sauer will provide instructions on how to access the serial number. The optic sights come in the color black and with one packaged CR2032 button cell battery.