The recall is in response to a problem with the device’s motor that causes chest compressions to stop, which has resulted in one injury and one death, according to an Aug. 22 news release from the FDA ...
Please provide your email address to receive an email when new articles are posted on . The FDA designated Defibtech’s recall of its automated continuous chest compression device as class I, the most ...
Aimee Slingerland, Defibtech’s Sr. Director of Sales for North America, demonstrates the new ARM XR Automated Chest Compression Device. Rugged, dependable, and with an unmatched battery life, ARM XR ...
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