After detecting positive samples of a rare-but-dangerous bacteria in multiple parts of the plant, the FDA closed the facility and Abbott announced a massive recall of its formula on Feb. 17.
Several FDA staffers reviewed the complaint in late October when it was sent to a regional FDA office, but an interview didn’t take place until two months later, in part due to the whistleblower’s scheduling conflicts. Califf also faced questions about why his agency didn’t anticipate the shortage, given that Abbott’s plant supplies roughly one-sixth of the U.S. formula supply. FDA did not contact the U.S. Department of Agriculture about a potential shortage until Feb. 11., just days before Abbott’s recall, according to Califf.
Nah. This isn't on the FDA. This is on Abbott. They couldn't even meet basic guidelines and determined it was better to close up than fix their stuff. The CEO of Abbott needs to be addressing Congress, not FDA.
Weird I been hearing is trump and all the republicans fault.
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