Field Day Organic Ranch Dressing packaged in an 8 fl. oz. glass bottle, UPC #042563600242. The lot code is located on the back of the bottle above the label. Specifically, the front label of the affected product is correctly labeled Field Day Organic Ranch Dressing, 8 fl oz. The issue is some bottles have an incorrect back label such that the contains statement does not list milk and egg as allergens. These bottles can be identified by UPC# 042563600259.

Class I - Dangerous
Recalled: September 14, 2016 Drews Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    Lot Code W210I, Best By date of Jan. 28, 2018
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. 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:
Drews LLC
Reason for Recall:
Undeclared milk and egg allergen.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Field Day Organic Ranch Dressing packaged in an 8 fl. oz. glass bottle, UPC #042563600242. The lot code is located on the back of the bottle above the label. Specifically, the front label of the affected product is correctly labeled Field Day Organic Ranch Dressing, 8 fl oz. The issue is some bottles have an incorrect back label such that the contains statement does not list milk and egg as allergens. These bottles can be identified by UPC# 042563600259.

Product Codes/Lot Numbers:

Lot Code W210I, Best By date of Jan. 28, 2018

Distribution:

Distributed in: IL

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0677-2017

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