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FDA Recalls Liquid Pharmaceutical Products

FDA Recalls Liquid Pharmaceutical Products

Later in September of 2017, the Food and Drug Administration (FDA) announced a recall of many liquid pharmaceutical products because of possible bacterial contamination. The products made by PharmaTech LLC in Davie, Florida, included liquid stool softeners, liquid vitamin D drops, and liquid multivitamins marketed for infants and children.

Earlier, there was a discovery of Burkholderia cepacia bacteria in both Diocto Liquid and Diocto Syrup, which prompted the recall by 3 companies that label Pharma Tech products (Rugby Laboratories, Major Pharmaceuticals, and Leader Brands).

The bacterial species poses a significant threat to vulnerable patients, particularly young patients, such as infants and young children, who still have developing immune systems. The products were sent nationwide to different retailers, healthcare facilities, pharmacies, and sold online.

Signs of infection can range from having no symptoms at all to severe respiratory infections. Bacterial infections can also spread from person to person through direct contact and can be resistant to conventional antibiotics. If you’re using any of these products, stop using them immediately. If you have questions, contact Rugby Laboratories/Major Pharmaceuticals at (800) 645-2158 or Leader at (800) 200-6313.

If you or a loved one were injured by a contaminated drug, don’t hesitate to get in touch with one of our San Francisco defective pharmaceuticals attorneys. Kaiser Gornick LLP has more than 50 years of combined legal experience to offer your case. If your injury was caused by negligence and led to piles of medical bills, lost wages, and pain and suffering, you might be eligible for compensation.

Contact us about your case by calling us at (855) 534-0061 or filling out our online form today.

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