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Blood Pressure Drugs Containing Valsartan, Irbesartan and Losartan Have Been Recalled Due to Possible Contamination by Cancer-Causing Chemicals.

Do you or a loved one take blood pressure medication?  If so, you should be aware of the latest FDA Recall Announcements for certain blood pressure drugs that contain valsartan, irbesartan and losartan. These popular blood pressure prescriptions are all part of a class of drugs called angiotensin II receptor blockers (ARBs).  Multiple manufacturers and distributers are recalling certain lots …

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Press Release: Victims of Alleged Undertreatment and Fraudulent Billing File a Class Action Claim Against The Toledo Clinic and Medical Providers

Today the law firm of Zoll & Kranz, LLC filed a class action complaint on behalf of class members allegedly billed for a greater amount than received of Botox injections from The Toledo Clinic and neurologists Auberle and Maiteh.    [Toledo, OH, August 2019] Today, August 13, 2019, the Complaint was filed in the Court of Common Pleas for Lucas …

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Benicar Settlement | Deadlines are Rapidly Approaching

  There has been a recent settlement announced for certain Benicar, Azor or Tribenzor claims. If you believe you may be entitled to compensation from an injury caused by these Olmesartan-containing medications made by Daiichi Sankyo, please contact our office today for a free consultation. Understand that there are urgent deadlines for eligible cases rapidly approaching and action must be taken …

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Invokana Warning Update: May increase risk of leg and foot amputations.

You may have read information on our website about the type 2 diabetes drug, Invokana. We have reported the potential risk and FDA warning with the alleged link to ketoacidosis injuries while taking Invokana. Recently, the FDA released a Safety Alert regarding a potential connection to an increased risk of leg and foot amputations. Also, Canagliflozin drugs, Invokana, Invokamet, and …

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Zimmer Biomet Recalls Their Comprehensive Reverse Shoulder Medical Device

The Comprehensive Reverse Shoulder device is being recalled by Zimmer Biomet because of a higher than expected device failure. The device was originally designed to help restore arm movement in patients with rotator cuff tears. Generally, these patients have experienced shoulder arthritis known as arthropathy. The manufacturer issued an Urgent Medical Device Recall Notice and a Certificate of Acknowdgement form …

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Safety Notice: A Medical Device Recall for Certain Smith & Nephew Femoral Hip Replacement Systems

Zoll & Kranz, LLC attorneys have learned of a medical device recall affecting certain hip replacement components. Patients should be aware of a manufacturer recall of parts of the Smith & Nephew, Inc. Modular SMF™ hip replacement system and the Modular REDAPT™ revision femoral hip system. According to a letter sent by the manufacturer to doctors, including orthopedic surgeons, these …

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MDL No. 2740 Created for Taxotere Lawsuits

A multidistrict litigation (MDL) has been created for lawsuits alleging permanent hair loss resulting from use of the chemotherapy drug Taxotere. On October 4, 2016, the United States Judicial Panel on Multidistrict Litigation (JPML) granted a motion to transfer and consolidate these cases after considering input from counsel for Plaintiffs and Defendants. Zoll & Kranz, LLC was one of the …

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International Agency Says Roundup is Probably Carcinogenic to Humans

Since the 1970s, Monsanto’s Roundup has been one of the most-used herbicides in the United States.  Roundup’s active ingredient is a compound called glyphosate, which is mainly used by agricultural workers to kill weeds that compete with crops.  Roundup is used in other sectors as well, including home gardening and lawn care. On March 20th, 2015, the World Health Organization’s …