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2014-09-19 23:08:16

On September 17, the FDA announced that Baxter International Inc. recalls one lot of Potassium Chloride Injection 10mEq per 100mL due to a labeling error on the shipping cartons. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers. San Diego, CA (PRWEB) September 19, 2014 AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on Potassium...

2014-09-15 23:10:01

On September 9, the FDA announced that it requested the recall of sterile drug products by Downing Labs (aka NuVision Pharmacy) due to lack of sterility. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers. San Diego, CA (PRWEB) September 15, 2014 AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on sterile drug products. Following a...

2014-09-09 23:01:17

A Class I recall designation by the FDA indicates that use of the recalled medical device may potentially lead to serious adverse reactions or death. Port Washington, New York (PRWEB) September 09, 2014 Parker Waichman LLP, a national law firm that has long been dedicated to protecting the rights of victims who have been injured due to medical devices, comments on a recall issued by DePuy Synthes of its Craniomaxillofacial Distraction System. Federal regulators recently deemed the matter...

2014-09-08 23:06:21

With the release of a recent JAMA Psychiatry study showing that psychiatric drugs send nearly 90,000 Americans to emergency rooms annually, Citizens Commission on Human Rights, the leading mental health watchdog, in its latest article says there is a need for consumers to search its Psychiatric Drug Side Effects Database to learn the documented risks of these drugs. Los Angeles, California (PRWEB) September 08, 2014 A recent JAMA Psychiatry study revealed that between 2009 and 2011, there...

2014-09-05 23:03:28

On September 2, the FDA announced that Solace International, Inc. is recalling all lots of Dermatend Original and Dermatend Ultra due to safety concerns. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers. San Diego, CA (PRWEB) September 05, 2014 AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on Dermatend Original and Dermatend Ultra....

2014-09-05 20:21:11

RANDOLPH, N.J., Sept. 5, 2014 /PRNewswire/ -- Pharmacy Creations has voluntarily recalled four product lots (see below) following testing results conducted by Front Range, Inc., its former independent testing laboratory, that indicated that the product lots may have the potential of not being sterile. Pharmacy Creations no longer uses Front Range, Inc. for testing of any kind for any of its formulations. Although we cannot be certain that the product subject to the recall is contaminated,...

2014-08-26 23:00:28

On August 22, the FDA announced that Gel-E Donut and Squishon 2 gel-filled products, by Children’s Medical Ventures, are recalled (Class I) due to complaints about visible mold. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers. San Diego, CA (PRWEB) August 26, 2014 AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on Gel-E Donut and...

2014-08-25 23:10:14

On August 20, the FDA announced that 696 CloverSnare 4-Loop Vascular Retrieval Snare devices, by Cook Medical, are recalled due to risk of loop to separate from shaft. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers. San Diego, CA (PRWEB) August 25, 2014 AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on CloverSnare 4-Loop Vascular...

2014-08-18 23:09:50

On August 11, the FDA advised consumers not to purchase or use Arize due to undeclared drug ingredient. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers. San Diego, CA (PRWEB) August 18, 2014 AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on Arize. The US FDA advised consumers on August 11, not to purchase or use Arize because it...

2014-08-13 23:09:49

On August 7, the US FDA informed consumers that two lots of RegeneSlim appetite control capsules, by Regeneca Worldwide, were recalled due to presence of DMAA. In light of this news, AttorneyOne, a recognized authority on law, updated the website providing detailed information to consumers. San Diego, CA (PRWEB) August 13, 2014 AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on appetite control capsules. The FDA...


Word of the Day
jument
  • A beast of burden; also, a beast in general.
'Jument' ultimately comes from the Latin 'jugum,' yoke.
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