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Texas Medical Malpractice Resources & Information

Gericare Eye Wash Recalled by FDA Due to Contamination

On February 1, 2018, the numerous reports against the Gericare Eye Wash brought the announcement from the FDA for a recall of this product on a consumer level. The reason behind this was the discovery of potential contamination that compromises the health of the user. Once this happened, Kareway Products, Inc. voluntarily recalled approximately 60 thousand lots of the wash and irrigation solution. This recall included notifying the hospitals and retails stores of the demand to remove the product from their inventory or supply shelves, and return it to Kareway Products. The process was anticipated to finish by January 29, [...]

Medical Malpractice in Texas: How Bad is It?

Health care providers, decked out in clean uniforms and working in well-scrubbed surroundings project an air of unimpeachable competence and trustworthiness. They perform modern miracles each day whether that’s treating a nasty infection or extending the life of a loved one with the latest surgical procedure. But the medical profession is not perfect. Doctors and hospitals make thousands of serious errors each year causing unnecessary death and suffering. Many of those errors go unreported. There is no law requiring doctors to publicly admit mistakes and few doctors will do so voluntarily. According to research published in 1999 by the National [...]

Diocto Medicine Recall Information

Popular Stool Softener Recalled Over Risk of Infection Rugby-brand Diocto Liquid – a stool-softening product manufactured by PharmaTech LLC (Davie, FL) – has been voluntarily recalled by the manufacturer over a risk of contamination. All Diocto Liquid NDC 0536-0590-85 is included as part of the recall. According to the Food and Drug Administration (FDA), PharmaTech LLC is taking measures to identify consumers who may have purchased the affected product and alert them of the recall. The recall follows at least two “adverse event reports” of Burkholderia cepacia infections from individuals who utilized the product. What is a Burkholderia Cepacia Infection? [...]

FDA Advises Discontinued Use of PharmaTech Liquid Products Due to Contamination

In a recent advisory alert, the Food and Drug Administration warned medical professionals and pharmacies against the continued use of any liquid products manufactured by PharmaTech LLC out of Florida. This advisory is due to the discovery of Burkholderia cepacia (B. cepacia) which can cause potentially severe reactions and infections in people, especially those with poor health already. Rugby Laboratories out of Michigan issues a voluntary recall after several complaints that the product might be linked to signs and symptoms, and in some cases, infection of B. cepacia. Some of the common signs and symptoms of the bacterial infection include [...]

Diocto Recalled Again for Infection Risk

Almost one year after a previous recall, Rugby Laboratories is issuing another voluntary recall of their Diocto syrup laxatives and stool softeners. All lots of the product are involved in this recall. Diocto Liquid, also known as docusate sodium, is a laxative given mainly to patients in the hospital recovering from heart attacks or surgery. The contaminated products were distributed to both retailers and hospitals. Stool softeners make it easier for the body to absorb water into the intestinal tract, thereby softening the stool so patients don’t experience pain or discomfort after surgery, trauma, or giving birth. Last year, Diocto [...]