A press release this week announced that Tylenol has recalled some batches of its chidren’s and infant liquid pain relievers, made between April 2008 and June 2008. The good news is that the issue, a contaminated inactive ingredient that did not make it into the final product, is not one likely to cause serious harm, according to the manufacturer. The company also has clearly released specific lot numbers that may be affected, so that concerned mothers and fathers can check bottles that they may still have at home.
What I can’t get over, a day after I first heard about this, is why the announcement is being made 17 months after manufacture of this product. What IF the children’s medicine had been affected, and caused illness? What about all the children and infants who had been given the medicine by well-intentioned parents in the meantime?
Clearly, I need to understand FDA and product safety standards better, because I just can’t let this go. Why did it take so long to announce a potential contaminant in children’s medication?