Banana Muffin, brand Surtidoras Bakery, net wt. 1.74 lbs., packaged in rigid plastic clam shell container. No UPC. The allergens declared in the INGREDIENTS statement: "ENRICHED WHEAT FLOUR SOYBEAN OILWHEYWHEAT GLUTENEGGS SOY FLOURSOYBEAN OIL AND WHOLE EGGS". The allergens declared in the CONTAINS statement: "CONTAINS: WHEAT, EGGS, AND SOY".

Class I - Dangerous

🍎 Food Recalled: March 2, 2019 Surtidoras Bakery Dairy & Eggs

What Should You Do?

Check if you have this product:
SELL BY Dates: 03/19/19 and includes up to 3/26/19.
Do not eat it: Even if it looks and smells fine, do not consume this product.
Throw it away or return it: You can return the product to the store for a full refund.
Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:: Surtidoras Bakery Inc
Reason for Recall:: The ingredients statement declared wheat, soybean oil, eggs, soy flour, soybean oil, and WHEY. The ingredients statement does not declare Milk as a source of whey and the Contains statement does not declare Milk.
Classification:: Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
Status:: terminated

Product Information

Full Description:

Banana Muffin, brand Surtidoras Bakery, net wt. 1.74 lbs., packaged in rigid plastic clam shell container. No UPC. The allergens declared in the INGREDIENTS statement: "***ENRICHED WHEAT FLOUR *** SOYBEAN OIL***WHEY***WHEAT GLUTEN***EGGS*** SOY FLOUR***SOYBEAN OIL AND WHOLE EGGS***". The allergens declared in the CONTAINS statement: "CONTAINS: WHEAT, EGGS, AND SOY".

Product Codes/Lot Numbers:

SELL BY Dates: 03/19/19 and includes up to 3/26/19.

Distribution:

Distributed in: WA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1283-2019

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