More medical news from FDA Recalls
Stewart's Shops Issues Allergy Alert On Undeclared Milk In Sportade Fruit Punch
FDA Recalls : October 26, 2016, 4:33 am
Saratoga Springs, NY-Stewart's Shops Corp. is recalling units of Stewart's Sportade Fruit Punch Isotonic Beverage 20 fluid oz. because they may contain undeclared milk. People who have an allergy to milk run the risk of serious or life-threatening allergic reaction if they consume this product.
Brownwood Farms Issues Allergy Alert On Undeclared Milk In Fruit Preserves And Fruit Butter Products
FDA Recalls : October 21, 2016, 10:47 am
Brownwood Farms of Williamsburg, MI is recalling approximately 260,000 total units of the listed products, because they contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction, if they consume these products.
Yoma Myanmar Tea Co. Issues Allergy Alert on Undeclared Peanuts in Yoma Myanmar Tea Salad Snack
FDA Recalls : October 18, 2016, 9:34 am
Yoma Myanmar Tea Co. of Allston, MA is voluntarily recalling the Yoma Myanmar brand "Tea Salad Snack" in Regular and Spicy, 7 oz., because the products may contain undeclared peanuts. People who have allergies to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.
Voluntary Recall Notice of McCormick 24 oz. Club Size Original Taco Seasoning Mix Due to Unlabeled Milk Allergen
FDA Recalls : October 17, 2016, 10:30 am
SPARKS, Md., October 5, 2016 - McCormick & Company, Incorporated is initiating a voluntary class I recall of 24 oz. Club Size McCormick® Original Taco Seasoning Mix, UPC 52100302461 with best by date codes between June 27, 2018 and September 16, 2018 due to an unlabeled milk allergen
Medtronic Announces Voluntary Recall of its Pipeline Embolization Device, Alligator Retrieval Device, X-Celerator Hydrophilic Guidewire, Ultraflow and Marathon Flow Directed Micro Catheters
FDA Recalls : October 17, 2016, 6:22 am
This voluntary recall is being conducted due to the potential separation and detachment of the polytetrafluoroethylene (PTFE) coating on parts of these devices. Should the PTFE separate from the delivery wire or stylets, PTFE particulate could enter the blood stream of the patient.