Mai’s Bakery, Inc. of Monterey Park, CA. is recalling its listed “Hopia Mongo” and “Moon Cake” products because they may contain undeclared egg. People who have allergies to eggs run the risk of serious or life-threatening allergic reaction if they consume these products.
FDA approves Zostavax vaccine to prevent shingles in individuals 50 to 59 years of age
The Food and Drug Administration (FDA) today approved the use of Zostavax, a live attenuated virus vaccine, for the prevention of shingles in individuals 50 to 59 years of age. Zostavax is already approved for use in individuals 60 years of age and older.
Seoul Shik Poom Inc. Issues Allergy Alert On Undeclared Egg In (Samlip) Red Bean Bread
Seoul Shik Poom Inc. of Englewood, NJ is recalling its 3 pack/2.82 oz packages of “Red Bean Bread” because they may contain undeclared eggs. People who have an allergy or severe sensitivity to egg run the risk of serious allergic reaction if they consume these products.
Shaping Beauty, Inc. Issues a Voluntary Nationwide Recall of Weight Loss Tea Found to Contain an Undeclared Drug Ingredient
outhampton, PA, Shaping Beauty,
Inc. has been informed by the Food and Drug Administration (FDA) that a weight loss
dietary supplement sold and marketed by the firm contain an undeclared drug ingredient.
FDA lab analyses of dietary supplement tea distributed by the company were found to
contain undeclared Sibutramine used as an appetite suppressant for weight loss. The FDA
has not approved the following products as drugs; therefore the safety and effectiveness
of this product is unknown. All lots of the following dietary supplement products are
being recalled
Unified Grocers Issues Allergy Alert on Undeclared Milk in Cottage Hearth Stone Ground Wheat Bread (24 oz) and 7 Select 100% Whole Wheat Bread (24 oz)
Unified Grocers is recalling Cottage Hearth Stone Ground Wheat Bread
(24 oz) and 7 Select 100% Whole Wheat Bread (24 oz) because they may contain undeclared
milk. People who have an allergy or severe sensitivity to milk may run the risk of serious or
life-threatening allergic reaction if they consume these products.
USA Far Ocean Group, Inc. Issues Voluntary Nationwide Recall of U-Prosta, a Product Marketed As a Dietary Supplement That Contains Undeclared Terazosin Hydrochloride
USA Far Ocean Group Inc., 1609 W. Valley Blvd., #338, Alhambra, CA 91803, announced today that it is conducting a voluntary nationwide recall of the Company’s supplement product sold under the name “U-Prosta Natural support for prostate health”. The Company has been informed by representatives of the U.S. Food and Drug Administration (FDA) that lab analysis by FDA of U-Prosta samples found the product contains terazosin, the active ingredient of an FDA-approved drug used to treat Benign Prostatic Hyperplasia (enlarged prostate), making U-Prosta an unapproved drug.
Del Monte Fresh Poduce Voluntairly Recalls Cantalopes Because Of Possible Health Risk
Del Monte Fresh Produce N.A., Inc. (“Del Monte Fresh”) of Coral Gables, Florida is voluntarily recalling 4,992 cartons of cantaloupes, each containing 4 plastic mesh sleeves with 3 cantaloupes per sleeve, because they have the potential to be contaminated with Salmonella Panama, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella Panama often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella Panama can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
Lakeside Foods Issues Recall of Nationwide Pickled Sliced Beets
Lakeside Foods, Inc. of Manitowoc, Wisconsin is initiating a voluntary recall of 3000 cases of
lOS-ounce canned pickled sliced beets because some cans may have been under processed. While no illnesses have been reported, these cans have the potential to be contaminated with
harmful organisms including Clostridium botulinum.
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FDA: Michigan heart-lung bypass machine manufacturer enters into consent decree
The U.S. Food and Drug Administration today announced that Terumo Cardiovascular Systems Corporation (TCVS) of Ann Arbor, Mich., and two of its officers, Mark A. Sutter, president and chief executive officer, and Mark Lincoln, vice president of Quality Assurance and Operations, have signed a consent decree of permanent injunction.
Millar Instruments, Inc. Issues a Recall of Millar Mikro-Tip Angiographic Catheter, Model SPC-454D and SPC-454F
Millar Instruments, Inc, Houston, Texas, is issuing a worldwide recall of 1,080 units of its Human Use
High Injection Angiographic Catheter. The Angiographic Catheter, Models SPC-454D and SPC-454F,
found to contain particulate debris within the catheter lumen, which potentially could result in
embolization of foreign debris to tissues, vasculature, and organs, potentially causing myocardial
infarction, stroke, limb ischemia, and /or death.