Les Chateaux De France, Inc., is recalling approximately 4,225 pounds of bacon-wrapped scallops due to misbranding and an undeclared allergen. The products contain milk, a known allergen, which was not declared on the product label. Use of this product may cause serious or life-threatening allergic reaction in consumers that are sensitive to milk.
This recall is for:
|G’s ITEM #||PRODUCT DESCRIPTION||MANUFACTURER ITEM#|
|82152||Bacon Wrapped Scallops||43|
Our Customer Service Department is in the process of contacting customers who have received this product.
Click here to see the official news release.
We adhere to the strict Hazard Analysis & Critical Control Points (HACCP) protocols to ensure product safety while in our possession. If a recall is issued by a manufacturer affecting our customers, our Recall Policy is implemented immediately, and all pertinent information is communicated to impacted customers by verbal contact as well as being posted here. You can also check www.foodsafety.gov for more information.
Recalls are actions taken by a firm to remove a product from the market. Recalls may be conducted on a firm’s own initiative, by FDA request, or by FDA order under statutory authority. Class I recall: a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. Examples of products that could fall into this category are a food found to contain botulinal toxin, food with undeclared allergens, a label mix-up on a life saving drug, or a defective artificial heart valve. Class II recall:a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. Examples of products that could fall into this category are a food found to contain botulinal toxin, food with undeclared allergens, a label mix-up on a life saving drug, or a defective artificial heart valve. Class III recall: a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences. Examples might be a container defect (plastic material delaminating or a lid that does not seal); off-taste, color, or leaks in a bottled drink, and lack of English labeling in a retail food. Market withdrawal: occurs when a product has a minor violation that would not be subject to FDA legal action. The firm removes the product from the market or corrects the violation. For example, a product removed from the market due to tampering, without evidence of manufacturing or distribution problems would be a market withdrawal.