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A study conducted by the non-profit Rand Corporation, among others reportedly found 36 published cases of non-Hodgkin’s lymphoma among women with breast implants. Although the links exist, the research does not conclusively prove that breast implants cause the cancer – specified as Anaplastic Large Cell Lymphoma – which may appear in several parts of the body including the lymph nodes, skin, bones, soft tissue, lungs or liver. But earlier this year, the FDA warned that a few dozen cased of…

Defibtech, LLC, the makers of the DDU-100 series Semi-Automatic External Defibrillator, has recently initiated a worldwide voluntary recall of the product. The defibrillator, sold under the names Lifeline AED and ReviveR AED, may fail to charge properly and then fail to do the intended job, which may, then, result in failure to resuscitate the patient. This action is a Class I recall, as defined by the FDA and the condition is not detectable by the periodic self test. Reports say…

A Maryland man was honored as a hero recently for jumping into a creek to save a boy from drowning. The man, Jack Severn, 71, of New Market, MD, was given a Heroism Medal from the Marine Corps League at the Maryland chapter’s annual convention in Ocean City, reports say. The man was at a Park in Frederick with his wife and granddaughter last month when a young boy fell into Carroll Creek. Severn jumped into the shoulder-deep water and…

The U.S. Food and Drug Administration recently issued a warning for Hem-o-Lok Ligating Clips, which are manufactured by Weck for living kidney donors. The clips keep the process of living donors — and recipients – from experiencing the potentially fatal problems associated with blood vessels not being properly closed after surgery. The process, reportedly called nephrectomy, is for kidney removal for kidney donor transplant surgery, and the FDA believes there may be concerns of serious risks to the organ donor….

Reports say that possibly 25-percent of Veterans Health Administration medical centers and its outpatient mail order pharmacy may have used defective alcohol prep pads – this despite a large and reasonably well-publicized U.S. recall of the products. The swabs, which were reportedly manufactured by Triad Group, issued several large-scale recalls for tainted alcohol swabs, alcohol swabsticks, prep pads, and other products sold under various brand names due to concerns for potential contamination with bacteria. The worries involve two specific bacteria,…