In the new warning letter sent to Perrigo, the FDA details that Cronobacter had been identified in finished formula products on multiple occasions by the company: in two products "during a ...

The Food and Drug Administration (FDA) sent warning letters to three infant formula manufacturers over violations of federal safety regulations, the agency announced Wednesday. ByHeart, Mead ...

Amazon has voluntarily pulled seven eye drop brands off their shelves in response to a warning letter issued by the Food & Drug Administration over potential safety concerns.. The eye drops ...

DexCom received a warning letter from the Food and Drug Administration following inspections of its San Diego and Mesa, Ariz. facilities and is working on a written response.

The warning letter followed an FDA inspection last year of Dexcom’s facilities in San Diego and Mesa, Arizona. Marcus wrote that after the FDA requested additional information and a separate 510 ...

The letter, which was issued Dec. 9, 2021, came after an inspection the FDA had conducted of the Northridge, California, facility the previous July—which in turn had been sparked by a pair of ...

Dexcom, the local maker of continuous glucose monitors, received a warning letter from the Food and Drug Administration last week citing issues at two of its manufacturing facilities.

The Food and Drug Administration issued a warning letter to Dollar Tree that said the retailer responded inadequately WanaBana's 2023 recall of apple cinnamon fruit puree pouches due to reports of ...

DexCom received a warning letter from the Food and Drug Administration following inspections of its San Diego and Mesa, Ariz. facilities and is working on a written response.