2010 Johnson & Johnson children's product recall

"[3] Foreign particles could potentially include solidified ingredients or "manufacturing residue such as tiny metal specks"[4] or mold.[3] The official FDA report, released May 4, said investigators found thick dust, grime, and contaminated ingredients at the manufacturing plant.[8] According to the FDA, consumers should stop using the recalled products even though the chance of related health problems was "remote."[3] A McNeil spokesperson stated that the recall was not made on "the basis of adverse medical events".[7] A dedicated website and telephone hotline were established by the company to handle customer inquiries.
product recallover-the-counter children's medicinesMcNeil Consumer HealthcareJohnson & JohnsonTylenolMotrinZyrtecBenadrylFort Washington, PennsylvaniaFood and Drug AdministrationBurkholderia cepaciaJamaicaPuerto RicoTrinidad and TobagoUnited Arab EmiratesChildren's MotrinHouse Committee on Oversight and Government Reform