Damon Industries recalls Bloody Mary Beverage Concentrate with Jalapeno Flavor due to unlabeled anchovies in Worcestershire sauce used in production. This poses an allergy risk for those with anchovy allergies.
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 Concentrate with Jalapeno Flavor because it contains anchovies that weren't listed on the ingredient label. This could cause allergic reactions in people sensitive to anchovies.
The juice product contains Worcestershire sauce made with anchovies that were not declared on the ingredient label. This means individuals with anchovy allergies could experience allergic reactions if they consume the product.
People who own or use this juice product are at risk if they have an anchovy allergy. The recall affects consumers who purchased this specific concentrate product.
Check for the product name 'Bloody Mary Beverage Concentrate with Jalapeno Flavor' with 59% juice content. The UPC code is 7 00073 02003 4. The product was manufactured by Damon Industries in Sparks, NV.
Look for the UPC code 7 00073 02003 4 on the product packaging.
The product contains anchovies that were not declared on the ingredient label, so it may pose a risk for people with anchovy allergies. Do not consume if you have an allergy.
Check for the product name 'Bloody Mary Beverage Concentrate with Jalapeno Flavor' with 59% juice content and UPC code 7 00073 02003 4.
Check the product label for the UPC code. If you have the product, you may want to avoid it due to the potential allergy risk.
We’ve drafted a message you can send Damon Industries to request your refund or repair — edit it as you like.
Subject: Recall F-1062-2015 — Damon Industries Damon Industries Hello, I own a Damon Industries that is covered by recall F-1062-2015 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.
