FDA recall: 2 popular coffee creamers sold in Mississippi are making people sick. Did you buy?
International Delight coffee creamer sold in Mississippi now under FDA recall. Did you buy them? Are they in your home? What ...
The U.S. Food and Drug Administration increases risk level to recalled coffee creamers
The Food and Drug Administration has increased the risk level of two coffee creamers recalled in late February. Approximately ...
Amazon Cookie Recall Now At FDA’s Deadliest Category—Is It A Risk?
The Amazon Fresh cookie recall is an FDA Class I recall due to undeclared egg allergens. Here’s why it took time to surface and if it may still poses a risk.
75,000 bottles of coffee creamer recalled by FDA in Ohio, US. See the full list
More than 75,000 bottles of International Delight coffee creamer are being recalled over concerns the product is spoiled.
MassDevice1d
FDA says Intuitive da Vinci 5 foot pedal recall is Class II
Class II recalls — a grade below the most serious Class I recalls — reference a situation in which the use of or exposure to ...
There's a Class II Recall on More Than 75,000 Bottles of International Delight Coffee Creamer Across 31 States
International Delight is recalling two popular coffee creamers—Cinnabon Classic Cinnamon Roll and Hazelnut—after reports of spoilage and illness. This recall affects nearly 76,000 bottles distributed ...
Muffin recall update as FDA issues highest risk warning
Muffins which were recalled in February have been issued the FDA's highest risk warning due to them having an undeclared allergen.
Manila Standard4d
FDA goes digital with eServices Portal System
THE Food and Drug Administration (FDA) has launched an online application process for Certificate of Medical Device ...
Modern Healthcare9d
FDA labels Philips' recall of Tack Endovascular Systems a Class I
Complications with the implant used to treat blood vessel dissection after balloon angioplasty or stent placement can result ...
Becker's Hospital Review11d
FDA issues class-wide labeling changes to testosterone products to include blood pressure, cardiovascular warnings
The FDA has announced new labeling changes for all testosterone products following a review of clinical trial data, including a TRAVERSE study and postmarket ambulatory blood pressure studies.