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 ...
Jun. 17—TIFTON — The Tift Regional Medical Center Foundation recently presented two Defibtech Lifeline ARMS — Automated Chest Compression Systems — to Tift County EMS and one to Turner County EMS.
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