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.”

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.”

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)

A production issue raised concerns that ink printing on some cups could run when exposed to high temperatures, inspectors said.

World Market is issuing a voluntary recall of a popular food spread because of a possible salmonella contamination in several states, including Texas.

YoCrunch yogurt products are being recalled nationwide by manufacturer Danone U.S., the U.S. Food and Drug Administration (FDA) announced Monday, July 14. The recall is due to the “potential presence of plastic pieces in the dome topper.”

All bottles of an ulcer medication have been recalled by the remains of a Kansas City drug company that filed Chapter 11 bankruptcy after paying millions to settle Medicaid fraud charges.