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Software Problems Prompt Computerized Anesthesia System Recall Ask any anesthesiologist about their job and they will likely tell you that the hard part is not putting patients to sleep, it’s getting them to wake back up. That is why Spacelabs Healthcare and the U.S. Food and Drug Administration (FDA) are recalling the ARKON anesthesia delivery system with Version 2.0 software due to (more...)

Anesthesia Care Computer System Recalled Over Deadly Glitch March 18, 2014 Some of the most serious cases of drug injuries occur when the wrong medication or dosage of a drug is given to patients. In some instances, these mistakes could be the result of hospital equipment malfunctions. The Defective Medical Device Lawyers with Ferrer Poirot Feller explain such a situation is why San (more...)

Drug Injury Lawyers Discuss The Effects of the Government Shutdown on Public Health October 15, 2013 The citizens of the United States depend on the federal government for the safety of the medications and medical devices we use on a daily basis. Since lawmakers have been mired in conflict, resulting in a government shutdown, many citizens have become concerned over who is examining and inspecting the products we (more...)

FDA Announces The Recall Of Another Defective Stryker Medical Device September 17, 2013 The Defective Medical Product Lawyers with the law firm of Ferrer Poirot Feller state that manufacturers of the products used by doctors during medical procedures have a responsibility to ensure the safety of the devices they release. Failure to do so could result in the company being held liable for any injuries (more...)