(March 20, 2017) New Hamburg, Ontario – EuroCan Manufacturing is voluntarily recalling Lot Number 84 consisting of it’s individually shrink-wrapped, 6-pack, 12-pack and 25-pack bags of Barnsdale Farms®, HoundsTooth® and Mac’s Choice® Pig Ears because they have the potential to be contaminated with Salmonella. Salmonella can affect animals eating the products and there is a […]
Yesterday, U.S. District Judge Marcia S. Krieger for the U.S. District Court for Colorado entered a consent decree of permanent injunction against EonNutra LLC, CDSM LLC and HABW LLC, manufacturers and distributors of unapproved drugs and dietary supplements, and their owner, Michael Floren, requiring Floren’s businesses to immediately cease operations until they come into compliance […]
Yesterday, U.S. District Judge Marcia S. Krieger for the U.S. District Court for Colorado entered a consent decree of permanent injunction against EonNutra LLC, CDSM LLC and HABW LLC, manufacturers and distributors of unapproved drugs and dietary supplements, and their owner, Michael Floren, requiring Floren’s businesses to immediately cease operations until they come into compliance […]
Nonna Foods in Woodbury, New York, is voluntarily recalling 25 ounce jars labeled as Lidia’s Marinara Sauce bearing a Best By Date 06/13/2019, because the product 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. Read The Complete Story!
BAK-EZ Bakery Company of Norcross, Georgia is recalling 7-Eleven 4.0 oz. Mantecada (Muffin) (SKU 9841) (UPC05254859241-7) because it may contain undeclared “milk” in the allergen statement. People who have an allergy or severe stativity to Milk they run the risk of serious or life-threatening allergic reaction if they consume this product. Read The Complete Story!
Regeneca Worldwide, a division of VivaCeuticals, Inc. is conducting a nationwide recall of its entire line of herbal and dietary supplement products pursuant to a Consent Decree entered by the federal court for the Central District of California. This recall applies to all products manufactured and sold between June 1, 2011 and February 8, 2017. […]
Biery Cheese Co. is voluntarily expanding the recall of specialty cheese due to potential contamination of Listeria monocytogenes. Deutsch Kase Haus, LLC of Middlebury, IN notified Biery Cheese Co. that a specialty Pepper Marble Jack cheese they supplied to Biery must be recalled due to potential contamination of Listeria monocytogens. Read The Complete Story!
Biery Cheese Co. is voluntarily expanding the recall of specialty cheese due to potential contamination of Listeria monocytogenes. Deutsch Kase Haus, LLC of Middlebury, IN notified Biery Cheese Co. that a specialty Pepper Marble Jack cheese they supplied to Biery must be recalled due to potential contamination of Listeria monocytogens. Read The Complete Story!
Meijer expanded its list of recalled items to now include its Meijer brand Artisan Made Natural Muenster Cheese and its pre-wrapped Ham Sub on Artisan White Baguette due to a potential cross contamination with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others […]
Meijer expanded its list of recalled items to now include its Meijer brand Artisan Made Natural Muenster Cheese and its pre-wrapped Ham Sub on Artisan White Baguette due to a potential cross contamination with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others […]
The U.S. Food and Drug Administration today approved Noctiva (desmopressin acetate) nasal spray for adults who awaken at least two times per night to urinate due to a condition known as nocturnal polyuria (overproduction of urine during the night). Noctiva is the first FDA-approved treatment for this condition.
The U.S. Food and Drug Administration today approved Noctiva (desmopressin acetate) nasal spray for adults who awaken at least two times per night to urinate due to a condition known as nocturnal polyuria (overproduction of urine during the night). Noctiva is the first FDA-approved treatment for this condition.
The U.S. Food and Drug Administration today approved Noctiva (desmopressin acetate) nasal spray for adults who awaken at least two times per night to urinate due to a condition known as nocturnal polyuria (overproduction of urine during the night). Noctiva is the first FDA-approved treatment for this condition.
The United States and the European Union (EU) completed an exchange of letters to amend the Pharmaceutical Annex to the 1998 U.S.-EU Mutual Recognition Agreement. Under this agreement, U.S. and EU regulators will be able to utilize each other’s good manufacturing practice inspections of pharmaceutical manufacturing facilities.
The United States and the European Union (EU) completed an exchange of letters to amend the Pharmaceutical Annex to the 1998 U.S.-EU Mutual Recognition Agreement. Under this agreement, U.S. and EU regulators will be able to utilize each other’s good manufacturing practice inspections of pharmaceutical manufacturing facilities.
The U.S. Food and Drug Administration today approved Odactra, the first allergen extract to be administered under the tongue (sublingually) to treat house dust mite (HDM)-induced nasal inflammation (allergic rhinitis), with or without eye inflammation (conjunctivitis), in people 18 through 65 years of age.
The U.S. Food and Drug Administration today approved Odactra, the first allergen extract to be administered under the tongue (sublingually) to treat house dust mite (HDM)-induced nasal inflammation (allergic rhinitis), with or without eye inflammation (conjunctivitis), in people 18 through 65 years of age.
Out of an abundance of caution and with an emphasis on customers’ wellness and safety, Yoke’s Fresh Market is proactively recalling two types of Colby cheese due to a potential contamination of Listeria monocytogenes. Read The Complete Story!
The U.S. Food and Drug Administration today approved Xermelo (telotristat ethyl) tablets in combination with somatostatin analog (SSA) therapy for the treatment of adults with carcinoid syndrome diarrhea that SSA therapy alone has inadequately controlled.