![]() For remediation of pump module door assembly replacement kits:.Remove the pump from service and send to biomedical engineering if pump module keypad lifting or stuck or unresponsive keys are observed.Do not spray fluids directly onto the device.Wring out the cleaning cloth to squeeze out excess fluid. Follow the cleaning instructions provided in the current Instructions for Use to minimize the potential for fluid entry during cleaning.In an urgent situation, close the roller clamp on the IV administration set to stop an infusion.Continue the infusion until it is safe to replace the PC unit if you are administering a critical medication.Remove the pump from service and send to your biomedical engineering staff if the pump module keypad shows signs of lifting, becomes unresponsive, or stuck.On March 3, 2021, CareFusion 303, Inc., sent a new urgent medical device recall letter to all affected customers and provided the following instructions: Actions for Clinical Users Although it had no reports of injuries or death, high-risk patient populations who are receiving life-sustaining infusions are at the greatest risk of harm, because delays or interruption of infusions can cause serious injury or death. The manufacturer received 79 reports of the keypad lifting up after fluid entry, which led to unresponsive or stuck keys, resulting in infusion delay or interruption or preventing clinicians from changing fluid or medication infusions on the affected devices. ![]() ![]() ![]() The recall is separate from the BD Alaris Pump Module 8100 keypad recall dated August 4, 2020. The parts were manufactured between January 15–Decemand distributed from January 23–December 5, 2019. ![]()
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