Recall of Another Children's Medicine Worries Philadelphia Parents
In the wake of Johnson & Johnson's recall of popular children's pain and allergy medicines, Blacksmith Brands, Inc. has just recalled four defective children's medicines sold in Philadelphia and across the nation. Philadelphia parents are warned to immediately stop using PediaCare Multi-Symptom Cold, PediaCare Long Acting Cough, PediaCare Decongestant and PediaCare Allergy and Cold medicines. The recalled PediaCare medicines were manufactured at the same facility implicated in the earlier Johnson & Johnson recall of 40 children's medicines, the largest recall of over-the-counter medications in history.
Food and Drug Administration investigators have uncovered a lengthy list of violations at the Fort Washington, Pennsylvania pharmaceutical plant where the recalled medicines were manufactured. Numerous manufacturing defects and quality control problems have been discovered, including higher concentrations of active ingredient than specified, inactive ingredients that do not meet testing requirements, and contaminants, most notably metal particles.
Philadelphia pediatricians warn that personal injury reactions to the contaminated medicines may include rash, diarrhea or vomiting. Philadelphia parents are cautioned to seek immediate medical attention if their child develops adverse symptoms after taking one of the recalled drugs. Parents should stop using the recalled drugs immediately.
In a Congressional hearing into the children's Tylenol recall last week, Food and Drug Administration officials strongly criticized Johnson & Johnson officials for failing to act quickly when problems were discovered with its over-the-counter drug operation. While drug companies are required to notify the FDA of consumer complaints within three days, Johnson & Johnson waited nearly a year to do so. The FDA began pressuring Johnson & Johnson to act in February when it was apprised of quality issues with over-the-counter children's medicines, yet the company did not recall defective products until April 30, and then only under extreme FDA pressure.
Adverse drug reactions can cause serious personal injury to infants and children. If your child becomes ill after taking a defective medicine, seek the advice of a Philadelphia personal injury lawyer.