The FDA stated that it is evaluating the risk of stroke, heart attack and death with FDA-approved testosterone products. Learn more.
Read more →
FDA warns against high-dose prescription acetaminophen Kim Painter, Special for USA TODAY 11:50 a.m. EST January 15, 2014 Concerns about liver damage lead to new warnings. Generic painkiller pills containing hydrocodone bitartrate and acetaminophen are shown at Oklahoma Hospital Discount Pharmacy in Edmond, Okla., in 2010. (Photo: […]
Read more →
FDA issues stern warning on Medtronic devices David Koenig, AP Business Writer 7:34 p.m. EST November 16, 2013 Defects in some guidewires for hearts are severe enough to cause injury or death, agency says. The “Rising Man” symbol stands in front of the Fridley, Minn.-based Medtronic. (Photo: […]
Read more →
Acetaminophen Is Leading Cause of Acute Liver Failure The dangers associated with the use of Tylenol or an acetaminophen product have long been known. However, the issue, in part, is whether the public was adequately informed of these risks. The story below discusses these risks. Published: […]
Read more →Applica Consumer Products Reannounces Black & Decker Spacemaker Coffeemaker Recall Due to Injury Hazard; Units Sold After Recall Consumers should stop using this product unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product. Recall date: August 15, 2013 Recall […]
Read more →
FDA warns of serious rash risk with acetaminophen pills Toni Clarke, Reuters Aug. 1, 2013 at 4:52 PM ET Tylenol and other painkillers containing the ingredient acetaminophen can cause potentially deadly rashes and blistering of the skin, U.S. health regulators warned on Thursday. Companies that sell prescription […]
Read more →
FOR IMMEDIATE RELEASE December 27, 2012 Release #13-083 CPSC Hotline: (800) 638-2772 CPSC Media Contact: (301) 504-7908 Four Retailers Agree to Stop Sale and Voluntarily Recall Nap Nanny Recliners Due to Five Infant Deaths WASHINGTON, D.C. – The U.S. Consumer Product Safety Commission (CPSC) and four major […]
Read more →
Medical Devices Medical Device Recalls Synthes Hemostatic Bone Putty Recall Class: Class I Date Recall Initiated: July 5, 2012 Product: Synthes Hemostatic Bone Putty Manufacturing Dates: July 6, 2011 – December 14, 2011 Distribution Dates: December 22, 2011 – June 25, 2012 The affected models and lot […]
Read more →
FDA and CPSC: Don’t Use Infant Sleep Positioners [fvplayer src=”https://dimartinilaw.comsample/wp-content/uploads/2012/05/FDA-and-CPSC-Dont-Use-Infant-Sleep-Positioners.mp4″ width=”640″ height=”480″] From: USFoodandDrugAdmin | February 01, 2011 | FDA and the Consumer Product Safety Commission (CPSC) are warning people not to use sleep positioners for their babies, because there is a chance they could suffocate. In […]
Read more →
Complications alleged from the use of AlloDerm AlloDerm® Regenerative Tissue Matrix (“AlloDerm”) is a biologic allograft product manufactured by LifeCell Corporation. Surgeons use AlloDerm in abdominal repair surgeries, hernia repair surgeries, and other reconstructive surgeries. There have been patient complaints of having experienced complications from the use […]
Read more →
