Check the Batch
Class ITerminated in FDA datasetRecall initiated Jul 25, 2019

The Milk Lady's Herbal Tea, packaged loose leaf in aluminum tin, net weight 2 oz or 56.5 grams.

Recalling firm: Mountain Mel's Essential Goods LLC

Why it was recalled

Herbal Tea product is recalled due to a potential contamination with Salmonella.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Nov 6, 2019.

Check your package

Compare the exact product and package details with the label you have.

ProductThe 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***".
Package size2 oz
UPC799632056584

FDA code information

Lot # ML6271950 Best By: 7/2021

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Full FDA record and distribution details

Original product 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***".

Extracted codes and context

TypeCode / valueContext
UPC799632056584l 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***
lotML6271950Lot # ML6271950 Best By: 7/2021

Original FDA recall reason

Herbal Tea product is recalled due to a potential contamination with Salmonella.

Recall details

Recall number
F-2098-2019
Event ID
83424
FDA status
Terminated
Initiated
Jul 25, 2019
Reported
Sep 11, 2019
Classified
Aug 30, 2019
Terminated
Nov 6, 2019
Quantity
10 units of 2 ounce tins
Location
Welches, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

CA, OR, and WA.

FDA source record · F-2098-2019

Data updated September 16, 2026. View official FDA data ↗

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