I Have A Headache After All These Johnson & Johnson Recalls – More Tylenol Products Were Recalled Today

The list of Johnson & Johnson recalls keeps on growing. Today, J&J and McNeil Consumer Healthcare unit announced that they recalled an additional 34,056 bottles of Tylenol 8 Hour Extended Release Caplets that were manufactured at their Fort Washington Pennsylvania plant before it was closed down. McNeil is issuing the recall after consumers complained of a musty odor in the packages. In addition, after a review of records, it was found that equipment cleaning procedures at the Pennsylvania plant may have been inadequate or not properly documented.

Over the past 15 months, J&J has recalled over 300 million bottles and packages of Sudafed, Tylenol, Benadryl, Sinutabs, Rolaids, Mylanta, and Motrin. In addition to their medication recalls, J&J also had to recall their defective DePuy hip implants.

As a physician and experienced product liability attorney I have witnessed the catastrophic injuries or wrongful deaths that can come from faulty, dangerous, contaminated or recalled drugs, medications, and medical devices. Since 1958, the experienced medical and legal teams here at the Beasley Law Firm have gone up against some of the most powerful drug companies and won. The nationally known Philadelphia product defect lawyers, have years of successfully represented the rights of injured consumers just like you or a family member. Our medical experience and legal knowledge has awarded our clients thousands of awards in the seven, eight or nine figure range. To date, we have billions, not millions, but billions awarded to our injured clients just like you or a loved one.

Our record of success speaks for itself. If you or a loved one has been injured due to a defective product or recalled medicine, contact one of our experienced Philadelphia drug recall attorneys at (215) 866-2424.


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