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Worldwide Recall Issued by Mavidon

By |2020-01-09T12:59:26+00:00January 9th, 2020|Local News, Medical Recalls, Recalls|

Announcement Issued by Mavidon: Hospital and clinics are to STOP using LemonPrep®, PediaPrep®, Wave Prep, & Cardio Prep that were manufactured by Mavidon in their Riviera Beach, FL Facility IMMEDIATELY due to potential contamination with Burkholderia cepacia. Mavidon is voluntarily recalling all lots of products manufactured at their facility including LemonPrep®, PediaPrep® and Wave Prep 4-ounce tubes and single use [...]

Recall Alert – Abbott’s (formerly St. Jude Medical’s) implantable cardiac pacemakers

By |2019-08-05T16:34:27+00:00August 5th, 2019|Medical Recalls|

An additional recall has been issued on August 5th 2019: Abbott (Formerly St. Jude Medical Inc.), Recalls Ellipse Implantable Cardioverter Defibrillators Due to Exposed Aluminum Wires That May Prevent Defibrillation Therapy The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries [...]

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Recall Changes on Valsartan, Losartan and Irbesartan

By |2019-05-09T13:30:55+00:00March 1st, 2019|Failure To Diagnose, Local News, Medical Malpractice, Medical Recalls, Uncategorized|

FDA updates on angiotensin II receptor blocker (ARB) recalls including valsartan, losartan and irbesartan IMPORTANT: Medications containing only amlodipine or hydrochlorothiazide (HCTZ) are not being recalled. Manufacturers are recalling medications containing amlodipine in combination with valsartan or losartan, and medications containing hydrochlorothiazide HCTZ in combination with valsartan or losartan. […]

FDA Warns Taking These Antibiotics Could Rupture Aorta

By |2019-01-08T21:20:10+00:00January 8th, 2019|Medical Malpractice, Medical Recalls, Negligence|

A U.S. Food and Drug Administration (FDA) review found that fluoroquinolone antibiotics can increase the occurrence of rare but serious events of ruptures or tears in the main artery of the body, called the aorta. These tears, called aortic dissections, or ruptures of an aortic aneurysm can lead to dangerous bleeding or even death.

Recall of Valsartan Tablets Due to Cancer Risk

By |2018-11-30T15:52:25+00:00August 9th, 2018|Local News, Medical Recalls, Recalls|

The recall has spread globally with Health Canada and the European Medicines Agency having also recalled drugs using valsartan provided by Zhejiang Huahai.  The valsartan tablets (dosages 40mg to 320mg) the FDA has recalled include products from the following drug companies: A-S Medication Solutions (labeled as Solco Healthcare) Bryant Ranch Prepack HJ Harkins Company Northwind [...]

Nationwide Recall – CVS Sinus Mist

By |2018-11-30T15:52:39+00:00August 9th, 2018|Local News, Medical Recalls, Recalls|

Product Quest Manufacturing LLC Issues Voluntary Nationwide Recall of CVS Health 12 Hour Sinus Relief Nasal Mist Due to Microbiological Contamination. For Immediate Release August 8, 2018 Contact Consumers Joan Sanger, Site Head of Quality  386-239-8787 Announcement View Product Photos Holly Hill, FL, Product Quest Manufacturing (“Product Quest”) is voluntarily recalling Lot# 173089J of CVS [...]