Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 229–240 of 3,846 recalls
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and additional contrast injection
Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and additional contrast injection
Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated occurrence of the suction button sticking.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.
Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to terminate the test.
Sterile anchors my lack sterility assurance.