All the products in the recall were sent to the US by BMS Foods in Indonesia, with FDA officials saying that contamination likely occurred during the packaging and preparation process. Tests have revealed that the shrimp may be contaminated with high ...

The Food and Drug Administration (FDA) has issued a major recall of popular deodorants sold nationwide. The recall, launched July 10, involves over 67,000 cases of Power Stick antiperspirant deodorants,

The recall of thousands of ramen noodles cases, issued after a labeling error, has been given the U.S. Food and Drug Administration's (FDA) second highest risk warning: a Class II. Kobayashi Noodle USA recalled 3,

From August 19, 2025, the FDA announced that B. Braun Medical Inc. (B. Braun) is voluntarily recalling 2 lots of its Lactated Ringer’s Injection, USP, 1000 mL and 0.9% Sodium Chloride Injection, USP, 1000 mL to hospitals because of the presence of particulate matter in the containers.

A trio of Indian drugmakers—Alembic Pharmaceuticals, Sun Pharmaceutical and Glenmark Pharmaceuticals—issued separate voluntary U.S. drug recalls in recent weeks due to either the presence of carcinogens or foreign matter in the products.

The U.S. Food and Drug Administration has elevated the recall of a dessert dip previously sold at Aldi to Class II, meaning that the "product may cause temporary or medically reversible adverse health consequences," per the FDA website.

The FDA said the request to quarantine the devices followed reports of the products “resisting shape retention when being bent.”