August 3, 2007 Two children in West Texas have been diagnosed with Botulism poisoning as a result of eating Castleberry’s Austex Hot Dog Chili Sauce Original for lunch on June 28. One is now hospitalized in critical condition. The day after eating the tainted Castleberry’s...
Heparin Sodium Injection Vials were recalled due to an increase in adverse Heparin reactions. Baxter has received 100 reports of negative reactions and one death that may be linked to the Baxter Heparin recall. A variety of Heparin-caused reactions have been reported such as burning...
It's a bit frightening to know that a six-ton moving truck with 234,000 miles on it had not been inspected before U-Haul leased the "Household Mover" to Talmadge Waldrip. An unsuspecting customer who was helping his daughter move, Waldrip was run over by the...
FDA issued a Public Health Advisory and a Healthcare Professional Sheet to alert healthcare professionals and consumers regarding concerns over the use of Fentora (fentanyl buccal) tablets after recent reports of deaths and other adverse events. The deaths reported were the result of improper...
August 3, 2007 Nearly one million Fisher Price toys were recalled due to the possibility of lead poisoning. The U.S. Consumer Product Safety Commission announced a voluntary recall of Sesame Street, Dora the Explorer, and other children's toys. The surface paints could contain high levels of...
The FDA announced that many consumers may not be aware of the May 2007 recall of Complete MoisturePlus Multipurpose Contact Lens Solution manufactured by Advanced Medical Optics (AMO) and continue to use the recalled product. Several cases of Acanthamoeba Keratitis have been reported to...
Chrysler says it's recalling nearly 600,000 Dodge trucks and vans. The company says it's addressing concerns that the vehicles could shift out of park without the key in the ignition. Chrysler says there have been nine incidents involving injuries connected to the problem, but no fatalities...
Thoratec Corporation and The US Food and Drug Administration (FDA) notified healthcare professionals and patients of a Class I Recall of Thoratec Implantable Ventricular Assist Devices (IVADs) Driver, serial numbers 488 and higher (located on the label of the sterile package and on the...
The Food and Drug Administration (FDA) informed healthcare professionals of reports of sudden decreases or loss of hearing following the use of PDE5 inhibitors, Viagra, Levitra, Cialis for the treatment of erectile dysfunction and Revatio for the treatment of pulmonary arterial hypertension. In some...
The Food and Drug Administration announced last they are finally looking into Chantix, a stop smoking medication, to find out how dangerous it might be. Since the report of Carter Albrecht's unusual behavior and death while taking Chantix, hundreds of other Chantix patients have spoken...
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