As such, the FDA has classified the New Mexico Pinon Coffee pod recall as a Class III risk. The FDA defines such a risk as “a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”

WASHINGTON - A.P. Deauville, LLC, has voluntarily recalled more than 67,000 cases of various Power Stick roll-on antiperspirant deodorants nationwide due to deviations from current Good Manufacturing Practice regulations, according to an enforcement report of the Food and Drug Administration.

More than 67,000 cases of roll-on deodorant from a popular brand have been recalled nationwide, according to the FDA.

Walmart has issued a spree of other recalls this month, including Oscar Mayer Turkey Bacon, RITZ Peanut Butter Cracker Sandwiches and YoCrunch yogurts. These recalls were issued over concerns of clear plastic shards within products, allergy mislabeling and possible listeria monocytogenes contamination.

The move is expected to cause a “near-term stock out of Bicillin L-A,” Pfizer said in its statement, with the drugmaker now allocating “limited quantities of inventory to customers during this period as we establish a path to full recovery.”

Renner discussed hallucinating visuals of Foxx and "talking to objects" with 'Jimmy Kimmel Live' guest host Jelly Roll

The Food and Drug Administration (FDA) upgraded a blueberry recall this week to the highest risk level amid concerns of contamination. The FDA raised the recall of 400 boxes that weigh 30

Note that some links may require registration or subscription. White House officials overrode NIH career staff in deciding which "dangerous gain-of-function research" projects on viruses and pathogens should be halted, including pulling funding for 11 tuberculosis studies originally deemed safe by scientific reviewers. ( Washington Post)