This classification is used when the FDA finds a reasonable chance that exposure could cause serious harm or death.
The FDA has flagged J&J Medtech’s recall of its Cerepak detachable coils as Class I in the wake of one death and four serious ...
It means the products may cause temporary or medically reversible adverse health consequences, according to the FDA.
A fault in J&J MedTech’s CEREPAK detachable coils, used in intracranial aneurysm embolisation procedures, has been associated ...
This is an archived article and the information in the article may be outdated. Please look at the time stamp on the story to see when it was last updated. TENNESSEE (WHNT) — The Federal Drug ...
The FDA classifies the recall as a Class II risk level—a moderate risk associated with the consumption of the recalled ...
The Food and Drug Administration has issued its most severe warning for fresh tomatoes sold in three states. A Class I recall is issued if there is a potential for serious health complications or ...