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Medical device and health technology recalls from FDA. Includes diagnostic equipment, implants, monitors, and therapeutic devices.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2 Oral-Nasal Filter Line/Intubated Filter (CO2) Line device users may experience difficulty/inability to disconnect adapter from endotracheal tube for procedures (e.g. suctioning), may cause treatment delay and/or unintended extubation, which could lead to respiratory failure, hypoxia, aspiration, and/or low oxygen saturation.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Due to a manufacturing issue, leadless pacemakers may have been exposed to higher than normal temperatures which may result in premature battery failure.
A problem was discovered during the scanning process of the outer carton label because of an incorrect GTIN on the label, which is a GTIN for a different product.
Airway adapter does not meet specification and may break off when attaching a valve or tube. Device failure may result in inaccurate readings, a break in airway circuit, and loss of ventilation. A break in the airway circuit could result in inability to ventilate, hypoxia, cardiopulmonary collapse, or death.
Potential breach in pouch packaging which could lead to loss of sterility.
The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.
The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
Potential breach in pouch packaging which could lead to loss of sterility.