FDA Recall United States Terminated Historical recordClass I
Mountain Mel's Essential Goods LLC
- Product
- Peaceful Baby For Colic & Teething Discomfort Herbal Tea, pa…
- Published
- September 11, 2019
- Distribution
- CA, OR, and WA.
Mountain Mel's Essential Goods LLC Recall: Herbal Tea product is recalled due to a potential contamination with Salmonella.
United States
TerminatedClass I
- Company
- Mountain Mel's Essential Goods LLC
- Product
- The Milk Lady's Herbal Tea, packaged loose leaf in aluminum…
- Recall date
- July 25, 2019
- Terminated
- November 6, 2019
- Source
- FDA
Reason for recall
Herbal Tea product is recalled due to a potential contamination with Salmonella.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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***". | Not published in this source record | 10 units of 2 ounce tins | Lot # ML6271950 Best By: 7/2021 |
Distribution
- CA
- OR
- and WA.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-2098-2019
- Event ID
- 83424
- Status
- Terminated
- Classification
- Class I
- Company
- Mountain Mel's Essential Goods LLC
- 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***".
- Quantity
- 10 units of 2 ounce tins
- Reason
- Herbal Tea product is recalled due to a potential contamination with Salmonella.
- Recall initiation date
- July 25, 2019
- Report date
- September 11, 2019
- Classification date
- Not published in this source record
- Termination date
- November 6, 2019
- Distribution pattern
- CA, OR, and WA.
- UPC, lot, and code information
- Lot # ML6271950 Best By: 7/2021
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 83424 with 2 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass I
Mountain Mel's Essential Goods LLC
- Product
- Diges-Teas Herbal Tea, packaged loose leaf in aluminum tin,…
- Published
- September 11, 2019
- Distribution
- CA, OR, and WA.
Responsible company: Mountain Mel's Essential Goods LLC
Other recalls from Mountain Mel's Essential Goods LLC
FDA Recall United States Terminated Historical recordClass I
Mountain Mel's Essential Goods LLC
- Product
- Peaceful Baby For Colic & Teething Discomfort Herbal Tea, pa…
- Published
- September 11, 2019
- Distribution
- CA, OR, and WA.
FDA Recall United States Terminated Historical recordClass I
Mountain Mel's Essential Goods LLC
- Product
- Diges-Teas Herbal Tea, packaged loose leaf in aluminum tin,…
- Published
- September 11, 2019
- Distribution
- CA, OR, and WA.
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| California | 1 |
| Oregon | 1 |
| Washington | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
