While neither warning is classified as a recall, the FDA has provided additional information for the two products. Boston Scientific told customers that its Endotak Reliance defibrillation leads with expanded polytetrafluoroethylene-coated coils could become calcified, the FDA said.

A Class II risk classification (one of three) refers to a situation in which the "use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote,

The Oregon-based company known for its sugar-free sweeteners is recalling NuNatural’s Organic Pure Stevia and Pure Monk Fruit Sweetener because 78 bottles of each – 156 in total – bear the