Chester County News and Community Website
WASHINGTON, D.C. — The Food and Drug Administration (FDA) has issued an alert regarding the recall of 840 units of Chocolate Fudge with Nuts by Authentik Fudge, a company based in …
FDA Alert: Mold Concerns Prompt Recall of Montreal Fudge by Authentik Fudge Read More
WASHINGTON, D.C. — The Food and Drug Administration (FDA) has announced a voluntary recall by Veata LLC of lot number 230811 of Endurance Pro Energy Boost capsules. The recall, prompted by …
FDA Recall: Endurance Pro Energy Boost Capsules Contain Undeclared Sildenafil Read More
WASHINGTON, D.C. — The Food and Drug Administration (FDA) has announced a voluntary recall by Boulla LLC of lot number 230811 of Boom Max capsules. These capsules, packaged in 10-count blisters …
FDA Announces Recall of Boom Max Capsules Due to Undeclared Sildenafil Read More
WASHINGTON, D.C. — The Food and Drug Administration (FDA) has announced a recall by Unilever in the United States for approximately 137,000 cases of Popsicle Jolly Rancher Frozen Confection Pops due …
Important Recall Notice: Popsicle Jolly Rancher Frozen Confections – Stay Informed Read More
WASHINGTON, D.C. — The Food and Drug Administration has announced a voluntary recall by Flagstone Foods, LLC, the manufacturer of Emerald Nuts, for its 6.5oz Emerald Kettle Glazed Walnuts. This recall …
FDA Announces Voluntary Recall of Emerald Kettle Glazed Walnuts Due to Undeclared Nuts Read More
WASHINGTON, D.C. — The Food and Drug Administration has announced a recall by Gutierrez Distributor of Passaic, NJ, involving El Servidor Corp brand ground cinnamon. The recall is due to potential …
FDA Announces Recall of El Servidor Corp Ground Cinnamon Due to Lead Contamination Read More
WASHINGTON, D.C. — The Food and Drug Administration (FDA) has revealed that El Chilar HF, LLC has initiated a recall of specific lots of its ground cinnamon product due to …
FDA Announces Recall of Ground Cinnamon Due to Lead Contamination Read More
WASHINGTON, D.C. — The Food and Drug Administration (FDA) has provided an important update regarding the ongoing recall of the Apple iOS t:connect mobile app by Tandem Diabetes Care, Inc. (Nasdaq: …
FDA Announces Update on Tandem Diabetes Care’s Recall of t:connect Mobile App Read More
WASHINGTON, D.C. — The Centers for Disease Control and Prevention (CDC) has issued an update on the ongoing multistate outbreak of Listeria monocytogenes infections. The latest data highlights an increase …
CDC Updates on Multistate Listeria Outbreak Linked to Boar’s Head Deli Meats Read More
WASHINGTON, D.C. — The Food and Drug Administration (FDA) has announced that Breas Medical is initiating a nationwide correction of 8,186 Vivo 45 LS ventilator devices. Internal testing identified the …
FDA Announces Nationwide Correction of Breas Medical Ventilators Due to Formaldehyde Exposure Risk Read More