Smart & Final of Los Angeles, Calif. is recalling 2.5 lb. La Romanella Tri-Color Cheese Tortellini because it may contain undeclared wheat, eggs and milk. People who have an allergy or severe sensitivity to wheat, eggs and /or milk run the risk of serious or life-threatening allergic reaction if they consume these products.
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Maple View Farm Recalls Three Flavors of Ice Cream Because of Undeclared Allergens
Maple View Farm is voluntarily recalling pint containers of Cookies & Cream, Carolina Crunch and Cookie Dough ice cream because the products contain allergens that were not declared on package labels. Some or all of the products contain wheat,soy, almonds and peanuts, which can cause serious allergic reactions in people who have an allergy or sensitivity to these ingredients.
Orville Redenbacher’s® Classic Kettle Korn Ready-to-eat Popcorn Recalled Due to Undeclared Milk Allergen
Today, ConAgra Foods, Inc., (NYSE: CAG) in cooperation with the U.S. Food and Drug Administration (FDA) is voluntarily recalling packages of its Orville Redenbacher’s Classic Kettle Korn flavor ready-to-eat popcorn that may contain an undeclared allergen, milk. Certain bags of the Kettle Korn flavored ready-to-eat popcorn may have inadvertently been filled with white cheddar flavored popcorn, which contains an allergen, milk.
Saratoga Therapeutics, LLC Issues Allergy Alert on Undeclared Milk Components in Eba Multivitamin Supplement
April 23, 2013 – Saratoga Therapeutics, LLC of North Wales, PA is recalling 900 bottles of ebA Multivitamin Supplement because they may contain undeclared milk components –milk protein(s) and lactose. The following lot numbers may be affected:
# 0912164 expiration date 12/12
# 1110354 expiration date 10/14
People with an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction and people who have lactose intolerance run the risk of gastrointestinal symptoms if they consume ebA Multivitamin Supplement.
Hospira Issues a Voluntary Nationwide Recall of One Lot of 0.9% Sodium Chloride Injection, USP, 100 ML, Flexible Containers Due to Particulate
Hospira, Inc. (NYSE: HSP), announced today that last August it initiated a voluntary nationwide user-level recall of one lot of 0.9% Sodium Chloride Injection, USP, 100 mL, Flexible Container, NDC 0409-7984-23. This action was due to one confirmed customer report where four separate particulate issues were identified in four individual flexible containers.
Potential for Delivery System Catheter Separation Prompts Cook Medical to Initiate Voluntary Global Recall of Zilver® PTX® Drug Eluting Stent
Based on its investigation into a small number of complaints that the delivery system of the device had separated at the tip of the inner catheter, Cook Medical has initiated a nationwide/global voluntary recall of its Zilver® PTX® Drug Eluting Peripheral Stent. Cook received 13 complaints of delivery system tip separation with an occurrence rate of 0.043 percent.
FDA launches partnership to protect against counterfeit anti-malarial medicines with FDA-developed handheld detection tool
The U.S. Food and Drug Administration today announced a public-private partnership to help identify counterfeit or substandard anti-malarial medicines, including falsified products, with the deployment of the FDA-developed Counterfeit Detection Device, called CD-3.
7th Heaven Bakeries Issues Allergy Alert on Undeclared Egg, Soy And Milk in Oatmeal Raisin Cookies
7th Heaven Bakeries, Oklahoma City, is recalling OATMEAL RAISIN COOKIES, because they may contain undeclared dry eggs, soy lecithin, and whey solids. People who have an allergy or severe sensitivity to eggs, soy and milk run the risk of serious or life-threatening allergic reaction if they consume these products.
Nationwide Voluntary Field Correction Action Issued for GE Healthcare’s Giraffe Incubator and Giraffe OmniBed with Servo Oxygen Control System
On January 8, 2013, GE Healthcare initiated a nationwide voluntary field corrective action of the Giraffe Incubator with a Servo Control Oxygen System and Giraffe OmniBed, which were manufactured from August 1, 2012 through December 20, 2012. Giraffe Incubators without a Servo Control Oxygen System are not impacted.
Nora Apothecary & Alternative Therapies Announces a Voluntary Multi-State Recall of All Sterile Compounded Products Due to a Lack of Sterility Assurance
Nora Apothecary & Alternative Therapies today announced a voluntary multi-state recall of all sterile drug products compounded by the pharmacy that have not reached the expiration date listed on the product. The compounded products that are subject to the recall are those products within their expiration date that were compounded and dispensed by the pharmacy on or before Friday, April 19, 2013.