Medicine

Recalls

The Food and Drug Administration (FDA) is recalling a dietary supplement by the name of Pentrexyl Forte Natural, distributed by Phoenix Import & Distribution, because the packaging is believed to be misleading and may be confused with an antibiotic. The product does not contain antibiotics, and use of it by people who are ill could delay treatment for serious illnesses.



Recalls

The Food and Drug Administration (FDA) is recalling potentially defective laboratory instruments used to measure electrolytes in body fluids because the instruments have been giving incorrect results. The recall is listed as a Class 1, which is the most serious type of recall the agency can issue and involves situations in which there is a reasonable probability that use of the products will cause serious adverse health consequences or death.



Recalls

The Food and Drug Administration (FDA) is recalling dietary supplements manufactured by Multi-Mex Distributor and packaged to look like antibiotics that are readily available in Mexico and are possibly familiar to Hispanic consumers. The recall follows a temporary restraining order filed by Texas Attorney General Greg Abbot against Multi-Mex and San Martin Distributing Inc. for unlawfully marketing and dispensing a dietary supplement.



Recalls

The U.S. Food and Drug Administration today announced that it is requiring manufacturers to put a Boxed Warning on the prescribing information for the smoking cessation drugs Chantix (varenicline) and Zyban (bupropion).




Recalls

Celebrities and stars may be raving about the benefits of colon cleansing but a gastroenterologist from Charlottesville, Virginia urges consumers not to buy into the hype.




Recalls

A new medical procedure to find polyps in the colon may hold promise, but kinks still need to be worked out, according to a report in MedPage Today. The new procedure, called a capsule colonoscopy, offers an alternative to the traditional colonoscopy in which a patient undergoes a bowel cleansing process before going under local anesthesia and having a flexible telescopic camera passed through the rectum and bowel.




Recalls

Salix Pharmaceuticals, makers of gastrointestinal drugs, is reporting a first-quarter loss, however sales of the company's products used to clean the bowel prior to colonoscopies enjoyed a 23 percent increase compared to first quarter 2008, according to The News & Observer.




Recalls

On December 11, 2008, the Food and Drug Administration (FDA) issued a "black box warning" to consumers and health care professionals that a rare but serious form of kidney failure, acute phosphate nephropathy, had been associated with the use of prescription oral sodium phosphate (OSP) products Visicol and Osmo Prep, both made by Salix Pharmaceuticals. The products are routinely prescribed for bowel cleansing prior to colonoscopy, radiographic procedures and surgery. Acute phosphate nephropathy is a rare but serious adverse event that is often permanent and may require chronic dialysis. The FDA expressed equal concern about the risks associated with over-the-counter (OTC) bowel clearing products such as Fleet Phospho-soda and Fleet Accu-Prep solutions.




Recalls

On December 11, 2008, the Food and Drug Administration (FDA) issued a "black box warning" to consumers and health care professionals that a rare but serious form of kidney failure, acute phosphate nephropathy, had been associated with the use of prescription oral sodium phosphate (OSP) products Visicol and Osmo Prep, both made by Salix Pharmaceuticals. The FDA expressed equal concern about the risks associated with over-the-counter (OTC) bowel clearing products such as Fleet Phospho-soda and Fleet Accu-Prep solutions.




Recalls

Colon cleansing. It's a popular health trend. But a recent Food and Drug Administration (FDA) announcement urges cleansers to steer clear of OTC laxatives as a way to bowel cleanse.