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Last updated on April 19, 2014 at 12:41 EDT

Latest MedWatch Stories

2014-04-17 23:14:05

On March 26, the FDA announced the recall of Bella Vi products by Pure Edge Nutrition because they contain undeclared drug ingredients. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers. San Diego, CA (PRWEB) April 16, 2014 AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on safety alerts for weight loss dietary supplements. As the FDA...

2014-04-15 23:15:02

The FDA advised consumers on April 11, not to use Infinity because it contains a hidden drug ingredient, sibutramine. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers. San Diego, CA (PRWEB) April 15, 2014 AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on safety alerts for weight loss products. On April 11, the US FDA advised...

2014-04-14 23:10:18

On April 11, the FDA advised consumers not to purchase or use Lite Fit USA as it was confirmed it contained sibutramine. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers. San Diego, CA (PRWEB) April 14, 2014 AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on safety alerts for medical products including weight loss products. As the...

2014-04-11 23:22:36

The FDA warned consumers on April 8, to immediately stop using Zi Xiu Tang Bee Pollen capsules by Guangzhou Zi Xiu Tang Biotechnology Co. Ltd, because there were found to contain undeclared drug ingredients. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers. San Diego, CA (PRWEB) April 11, 2014 AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from...

2014-04-09 23:30:11

The FDA announced on March 20, that 56 lots of Pleo homeopathic drug products by Terra-Medica are recalled because they have the potential to contain penicillin. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers. San Diego, CA (PRWEB) April 09, 2014 AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on safety alerts for medical products...

2014-04-07 23:29:00

As the FDA announced on March 31, specific Nova Products Inc. dietary supplements for sexual enhancement are recalled because they were found to contain undeclared drug ingredients. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers. San Diego, CA (PRWEB) April 07, 2014 AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on safety alerts...

2014-03-17 16:28:56

PLEASANTON, Calif., March 17, 2014 /PRNewswire/ -- On March 4, 2014, Thoratec Corporation initiated a voluntary worldwide Medical Device Correction in order to update its labeling and training materials for the HeartMate II(®) LVAS Pocket System Controller (the "Pocket Controller"). The following information is provided as a reinforcement of the initial release. Failure to completely connect the driveline during the process of exchanging Pocket System Controllers has resulted in serious...

2014-03-14 12:28:50

LEXINGTON, Massachusetts, March 14, 2014 /PRNewswire/ -- Shire Pharmaceuticals announced today the initiation of a voluntary recall in the United States of one batch, packaged into three lots, of VPRIV due to the presence of visible particulate matter, identified as stainless steel and barium sulfate. The particulate matter was found in a small number of vials in the three packaged lots of VPRIV. A Shire investigation identified the particulate matter root cause as the third...

2014-03-04 16:26:01

PLEASANTON, Calif., March 4, 2014 /PRNewswire/ -- On March 4, 2014, Thoratec Corporation initiated a voluntary worldwide Medical Device Correction in order to update its labeling and training materials for the HeartMate II(®) LVAS Pocket System Controller (the "Pocket Controller"). This safety advisory is being issued because some patients and caregivers have experienced difficulties with the process of changing from a primary system controller to their backup system controller. These...

2014-02-19 12:28:02

MURRYSVILLE, Pa., Feb. 19, 2014 /PRNewswire/ -- Respironics, Inc., a Philips Healthcare business, today announced a worldwide recall of approximately 600 Philips Respironics Trilogy Ventilators, comprising Trilogy Ventilator Models 100, 200 and 202. (Photo: http://photos.prnewswire.com/prnh/20140219/NE67640-a ) (Logo: http://photos.prnewswire.com/prnh/20140219/NE67640LOGO-b ) On February 11, 2014, Philips Respironics initiated a voluntary recall to address a potentially defective component...