Damon Industries recalls Bloody Mary Beverage due to unlabeled anchovies in Worcestershire sauce used for mixing. This poses an allergy risk for those with anchovy allergies. Consumers should check product labels and contact Damon for details.
Firm discovered that Worcestershire sauce used in making various drink mixes contains anchovies which were not declared on the ingredient label or Allergan information.
Damon Industries is recalling Bloody Mary Beverage products because they contain anchovies that weren't listed on the ingredient label. This could cause allergic reactions in people sensitive to anchovies.
The beverage uses Worcestershire sauce that contains anchovies, which were not declared on the ingredient label or Allergan information. This means individuals with anchovy allergies could experience allergic reactions if they consume the product.
People who consume Bloody Mary Beverage products made by Damon Industries are at risk if they have anchovy allergies. This recall affects consumers who bought the product between the manufacturing dates listed.
Check for the product name 'Bloody Mary Beverage' with 56% juice content. Look for UPC codes 70073874057 (5-gallon bag) or 700073874125 (36 fl oz). The product was manufactured by Damon Industries in Sparks, NV.
Look for the ingredient label that lists anchovies or contact Damon Industries for confirmation.
The product contains anchovies that were not declared on the ingredient label or Allergan information, which could cause allergic reactions in people sensitive to anchovies.
Check the product label for anchovies or contact Damon Industries for further instructions.
The recall notice does not specify a deadline for action.
We’ve drafted a message you can send Damon Industries to request your refund or repair — edit it as you like.
Subject: Recall F-1068-2015 — Damon Industries Damon Industries Hello, I own a Damon Industries that is covered by recall F-1068-2015 from Damon Industries. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
