The recall of the Duloxetine Delayed-Release Capsules, produced by Towa Pharmaceutical Europe, was initiated on October 10 ...
The Food and Drug Administration (FDA) has upgraded an ongoing egg recall to Class 1, its highest categorization, signaling ...
Officials are continuing to warn consumers about an ongoing egg recall that has now been upgraded to Class I, meaning that ...
The vegetable products were recalled due to a possible contamination with the bacteria Listeria monocytogenes.
The recall, affecting eggs sold in three states, can cause "serious adverse health consequences or death," the FDA says.
Lunds & Byerlys Lone Star Dip products are being recalled over "potential mold growth contamination," according to the FDA.
Nearly a month after the Food and Drug Administration (FDA) issued an initial recall of eggs produced by a Wisconsin-based ...
Conducting a recall is a time-sensitive process that requires an informed, strategic, and measured approach. When conducting ...
The Food Safety and Inspection Service, an agency of the USDA, has continually updated a list of the brands products impacted ...