Fannie May Confections Brands, Inc. (“Fannie May”) is recalling 19 units of its 14.0 oz., rectangle box of spring wrapped assorted chocolates because the box includes one piece of candy that contains peanuts, a known allergen, and the food ingredient label on the box did not state that the product contained peanuts. Fannie May decided to recall the products after this was discovered during an internal review of product.
Infinite Herbs, LLC Voluntarily Recalls One Lot of Basil Organic Clamshells Because of Possible Health Risk
Infinite Herbs LLC of Miami, Florida is voluntarily recalling one lot of its 2.5 ounce packages of Organic Basil because of potential contamination with Salmonella. Salmonella is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.
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Abbott Issues Recall of Certain Blood Glucose Monitoring Systems
Abbott is voluntarily conducting a recall for the FreeStyle® Blood Glucose Meter and the FreeStyle Flash® Blood Glucose Meter. These two meters have not been in production since 2010.
SNI National is Voluntarily recalling Kratom XL 4 Pack, Maeng Da Kratom 10 Pack, Max Kratom 20 Pack, and Bali Kratom 40 pack Due to Undeclared Drug Ingredients
SNI National is voluntarily recalling all Kratom products,including Kratom XL 4 Pack, Maeng Da Kratom 10 Pack, Max Kratom 20 Pack, and Bali Kratom 40 Pack, from distributors and retail locations. These products contain Kratom (Mitragyna Speciosa).
Shire Pharmaceuticals Initiates Voluntary Nationwide Recall of One Batch, Packaged into Three Lots, of VPRIV® (velaglucerase alfa for injection)
Shire Pharmaceuticals announced today the initiation of a voluntary recall in the United States of one batch, packaged into three lots, of VPRIV due to the presence of visible particulate matter, identified as stainless steel and barium sulfate. The particulate matter was found in a small number of vials in the three packaged lots of VPRIV.
La Compania Pain Free by Nature Retira del Mercado las Tabletas de Reumofan Plus Debido a Ingredientes Medicos no Declarados
Woodland Park, CO Pain Free By Nature esta retirando del mercado las tabletas “Reumofan Plus” de venta a traves de su sitio web en www.painfreebynature.com, debido a que contienen ingredientes farmaceuticos activos no declarados: metocarbamol y diclofenaco. El uso de este producto puede resultar en danos graves y potencialmente mortales.
Dole Fresh Vegetables Voluntarily Recalls Limited Number of Bagged Salads Due to Possible Health Risk
Dole Fresh Vegetables is voluntarily recalling a limited number of cases of bagged salad. The products being recalled are Dole Italian Blend (UPC 7143000819), Fresh Selections Italian Style Blend (UPC 1111091045), Little Salad Bar Italian Salad (UPC 4149811014) and Marketside Italian Style Salad (UPC 8113102780) coded A058201A or B, with Use-by date of March 12, 2014 due to a possible health risk from Listeria monocytogenes.
Kirkland Signature Real Sliced Fruit Recalled Due to Possible Health Risk
Oregon Freeze Dry, Inc. of Albany, OR has voluntarily recalled 59,780 cases of Kirkland Signature Real Sliced Fruit, produced exclusively for Costco Wholesale Stores. In cooperation with Costco, the company issued the recall after determining the product has the potential to be contaminated with Salmonella.
Pain Free by Nature is Voluntarily Recalling Reumofan Plus Tablets Due to Undeclared Drug Ingredients
Pain Free By Nature is recalling “Reumofan Plus” Tablets purchased through their website at www.painfreebynature.com, because they contain undeclared active pharmaceutical ingredients: methocarbamol and diclofenac. Use of this product could result in serious and life-threatening injuries.
Greatbatch, Inc. Issues Voluntary Field Corrective Action for Standard Offset Cup Impactor
Greatbach, Inc. initiated a voluntary field corrective action for all Standard Offset Cup Impactors after an internal review determined that the sterilization recommendation in the Instructions for Use for the product did not meet requirements for sterility assurance, which has the potential to result in surgical infection. No incidents have been reported during clinical use of the product, nor have there been any reported adverse events.