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Nationwide sweetener recall update as FDA issues risk warning
NuNaturals, Inc. initiated a voluntary recall for select lots of its Organic Pure Stevia and Pure Monk Fruit Sweetener on ...
FDA raises recall of 64,800 lbs. of butter to second-highest warning level
Missouri-based food company Bunge North America has recalled 64,800 pounds - the equivalent of 1,800 cases - of its NH ...
Nationwide honey recall update as FDA issues risk warning
The FDA 's classification of the Queen Bee Gardens recall as Class II signals a moderate health risk, indicating that use or ...
FDA Elevates Recall of 64,800 Lbs. of Butter to Second-Highest Warning Level
Bunge North America Inc. initially issued a voluntary recall of 64,800 lbs. of its European Style Butter Blend on July 14 ...
FDA Issues Nationwide Class II Recall on 32 Tons of Butter
The U.S. Food and Drug Administration (FDA) has elevated a nationwide recall covering 64,800 pounds (that’s 1,800 cases) of ...
FDA upgrades nationwide butter recall alert to a higher level
( NewsNation) — The Food and Drug Administration (FDA) has escalated a recent nationwide recall of 64,800 pounds of butter to ...
Cookie Recall Update As FDA Issues Risk Warning
Reisman Bros Bakery originally announced a recall of various products distributed to nine states because of potential ...
FDA flags problems with two Boston Scientific heart devices tied to injuries and deaths
The agency said Wednesday an issue with defibrillator wires could cause the implants to fail to deliver adequate electrical shocks.
FDA raises recall of more than 64K pounds of butter to second-highest warning level
The U.S. Food and Drug Administration (FDA) has elevated the risk classification of a butter recall to the second-highest ...
Fish Recall Sparks FDA Risk Warning
Moon N Sea Ga Llc. issued a voluntary recall on June 24 for various fish products after they were potentially produced under ...
MassDevice1 天
FDA issues notice for another serious Philips Respironics ventilator recall resulting in deaths
The FDA has issued a notice warning of a device correction related to ventilators from Philips Respironics. This marks the ...
FDA recalls over 67,000 cases of Power Stick deodorant due to manufacturing violations
On July 10, Pennsylvania-based health and beauty manufacturer A.P. Deauville announced a recall of 67,214 cases of its Power ...