Birdy 3-in-1 Coffee Mix (Robusta) Recall [US]


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US/Silver Spring: FDA Logo BlueFood Gusto, Inc. recalls certain batch/lots of Birdy 3-in-1 Coffee Mix (Robusta) due to undeclared milk, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention. FDA: http://ht.ly/fEOq300wCp2

Direct link: http://www.fda.gov/Safety/Recalls/ucm501808.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Coffee Mix is subject to this recall:

  • Birdy 3-in-1 Coffee Mix (Robusta), sold in plastic pouches 18 by 27 by 16.5 grams (445.5 grams in total per package) and marked with lot number D092121515 on the Nutrition Fact Label.

According to the FDA, Food Gusto has recalled certain batch/lots of 3-in-1 Coffee Mix (Robusta) because the product contains undeclared milk, a known allergen and source of dietary intolerance. The area of known distribution is Massachusetts, Connecticut and New York.

==> For information about Milk Allergy or Lactose Intolerance, please consult the “Allergens & Intolerances” tab at the top of this page.

If you believe you have purchased or have in your possession any of the recalled Coffee Mix and could be allergic to its milk ingredients, have a close family member who is allergic or has previously experienced Anaphylaxis or are unsure of your allergy status, please do not consume it directly nor use it as an ingredient in another dish or preparation. Instead, return the product to the store where you purchased it for a full refund.

If you have any questions about this recall, please contact 1-862-264-6774 from 8:30 AM to 5:00 PM Eastern Standard Time.

==> To see other recalls and notifications caused by undeclared milk, please search for “milk” using the Search Box at the top of this page.

Want to read more about this recall? Please click on the links above to visit the originating site.

Want to read more about other recalls? Please click on the links below.

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Additional information about this recall:
Recalls Direct RIN: 7033-2016
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