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The Milk Lady's Herbal Tea, packaged loose leaf in aluminum tin, net weight 2 oz or 56.5 grams. UPC: 7 99632 05658 4. The label is read in parts: "***The Milk Lady s FOR GREATER MILK FLOW & CALM NERVES***CAFFEINE-FREE HERBAL TEA*** Mountain Mel s Essential Goods, LLC Welches, OR 97067***Supplement Facts***Fennel*** Directions: Drink 1-4 cups daily as needed. Steep 1-2 teaspoons in 8 oz. of hot water for 10-20 minutes***".

Class I - Dangerous
Recalled: July 25, 2019 Mountain Mel's Essential Goods Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    Lot # ML6271950 Best By: 7/2021
  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:
Mountain Mel's Essential Goods LLC
Reason for Recall:
Herbal Tea product is recalled due to a potential contamination with Salmonella.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

The Milk Lady's Herbal Tea, packaged loose leaf in aluminum tin, net weight 2 oz or 56.5 grams. UPC: 7 99632 05658 4. The label is read in parts: "***The Milk Lady s FOR GREATER MILK FLOW & CALM NERVES***CAFFEINE-FREE HERBAL TEA*** Mountain Mel s Essential Goods, LLC Welches, OR 97067***Supplement Facts***Fennel*** Directions: Drink 1-4 cups daily as needed. Steep 1-2 teaspoons in 8 oz. of hot water for 10-20 minutes***".

Product Codes/Lot Numbers:

Lot # ML6271950 Best By: 7/2021

Distribution:

Distributed in: CA, OR, WA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-2098-2019

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