Tylenol Recalls and Liver Failure
The popular over the counter painkiller Tylenol® has been the subject of recalls due to quality and manufacturing problems. Since 2009, McNeil Consumer Products/Janssen (subsidiaries of Johnson & Johnson) has recalled different formulations of Tylenol® worldwide for a variety of problems that could affect patient health including in some cases liver failure. Elevated levels of acetaminophen above the dosage listed on labeling have been documented in some of the formulations, increasing the risks.
Consumers are advised to discontinue use of Tylenol if there is an unusual odor or if the lot number is included on this list of Johnson & Johnson recalled products. Although the recalled products have been removed from stores, consumers may still have previously purchased Tylenol.
If you have taken one of the products from the recalled lots, keep the intact product bottle, box, or blister pack with the lot, expiration date and any remaining product.
If you have experienced side effects including liver failure or abnormal liver enzymes during or after taking Tylenol®, contact our office immediately at 888-55-HARMAN to learn more about your legal rights and potential compensation for injury. You may also fill out the inquiry form here.
Harman Law Firm offers no cost, no obligation consultations to consumers who believe they may have been harmed by defective drugs, devices, and consumer products.
Related information
“Janssen’s manufacturing problems may lead to criminal charges in Korea” by Dan Stanton, in-pharmatechnologist.com, May 20, 2013
“J&J dealing with OTC manufacturing issues on 3 continents” by Eric Palmer, Fierce Pharma Manufacturing, May 6, 2013
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Prozac linked to Birth Defects
Prozac is an antidepressant made by Eli Lilly and Company.
Scientists have found a potential connection between Prozac and birth defects.
If you took Prozac while you were pregnant and then gave birth to a child with a birth defect, please contact us immediately.
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Fosamax & Leg Fractures
If you have suffered a femur fracture while taking Fosamax, please contact us.
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DePuy Hip Implants Recalled
Federal authorities now examining other models of DePuy hip implants for safety, including the DePuy Pinnacle.
In September 2010, DePuy Orthopaedics recalled its ASR XL Acetabular System and ASR Hip Resurfacing Platforms.
Harman Law LLC represents patients who have DePuy hip implants.
If you or a loved one has a DePuy hip implant, please contact us today by completing a brief questionnaire, or by calling our toll free number (1-888-554-2762) for a free, no-cost no-obligation evaluation of your situation.
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Risperdal Linked to Gynecomastia
Risperdal® (Risperidone) is an atypical antipsychotic drug which has been linked to serious and potentially permanent side effects such as:
Gynecomastia – boys developing breasts.
Tardive Dyskinesia – uncontrollable movement of face, tongue, and mouth.
Heart attack from heart attack (cardiac arrhythmias and other cardiac causes).
Diabetes.
We are investigating the link between Risperdal and gynecomastia (breast development in boys and adolescent males).
If you or a loved one has suffered from gynecomastia, please contact us today for a free, no-cost no-obligation evaluation of your situation.
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