The Food and Drug Administration has updated their recall of a batch of Dubai chocolate spread to Class I, their highest level, due to risk of salmonella contamination.

Dexcom recalled certain glucose monitoring receivers that may fail to make an alert sound when blood sugar is dangerously low or high, the FDA said. The issue has been linked to 56 injuries.

The Food and Drug Administration July 15 announced a recall by Sandoz on certain lots of cefazolin, due to the lots being mislabeled as penicillin G potassium. The FDA said the inadvertent administration of cefazolin following a recommended dosage of penicillin G potassium could pose serious and potentially life-threatening health consequences.

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

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

FDA recalls Dexcom glucose monitors (G6, G7, ONE models) due to alert issues posing severe health risks. Read more here.

Prestige Consumer Healthcare Inc. issued a voluntary recall for more than 10,000 cases of honey cough syrup on June 17.

The Centers for Disease Control and Prevention and the U.S. the Food and Drug Administration are investigating a Salmonella outbreak in several states linked to recalled frozen sprouted beans.