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Indiana Injury And Family Lawyer Blog

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Recall of Roman Shades Due to Strangulation Scare

Roman Shades have been recalled by several companies over recent months following reports of strangulation in children the used the blind chords. Most recently, Ethan Allen joined the recall to include over 150,000 Roman Blinds. There were no reports of injury. However, all people using the Roman blinds should immediately…

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Construction Accidents: Know the Hazards

Construction accidents can be some of the most devastating types of accidents. Workers that are injured on the job may be eligible for worker’s compensation benefits. However, benefits offered through worker’s compensation may not equate to compensation for the total damages and life changing experiences that are incurred because of…

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Cardiac Patients: Class One Medical Device Recall

Cardiac patients should be aware of the Class I Recall involving Thomas Medical Products with the company’s Transseptal Sheath Introducer Kit, also known as HeartSpan, CHANNEL FX, and Torflex, Braided Guiding Introducer Kit. This medical device is used in cardiac patients to pass a heart catheter from one side of…

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Dialysis System Recall: Baxter Healthcare Faced with Class I Recall

Dialysis Systems by Baxter called HomeChoice and HomeChoice PRO are under a medical device recall following reports from physicians that people have experienced serious injury and one known death because of a defect in the product. The specific defect is unknown at this time. What is known is that the…

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Food Borne Illness Risk Uncovered at Meyer Food Service Plant

Food borne illnesses can be traced to manufacturing plants that do not meet regulations for safety. Red flags went up for the risk of a food borne illness at Meyer’s Seafood Processing Facility recently. In October of 2009, inspectors uncovered violations of the seafood Hazard Analysis and Critical Control Point…

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Closed IV Catheter Systems Recall

Millions of Becton, Dickinson and Company catheter systems are involved in a recall because of a defect in the product that may result in injury or death to a user. The direct flaw of the catheter system involves the risk of an air embolism and leakage of blood or therapeutic…

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Cardiac Defibrillator Recall

Cardiac defibrillators can be faulty at times and such is the case with Cardiac Science’s automated external defibrillator. The manufacturer of the medical device has discovered a flaw in the design of the defibrillator which can lead to the inability to resuscitate an individual in need. Over 12,000 of the…

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