Mountain Meadow Herbs, Inc. Recall: Product bottle has potential to become pressurized over time. When consumer opens a bottle, the cap, capsules, and product powder could be forcefully expelled, and customers may sustain injuries to their hands and eyes. - F-0272-2022
United States
TerminatedClass I
- Company
- Mountain Meadow Herbs, Inc.
- Product
- Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3,…
- Recall date
- November 16, 2021
- Terminated
- January 11, 2022
- Source
- FDA
Reason for recall
Product bottle has potential to become pressurized over time. When consumer opens a bottle, the cap, capsules, and product powder could be forcefully expelled, and customers may sustain injuries to their hands and eyes.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3, 500 mg per capsule, 240 capsules per bottle. UPC 8 13086 01593 2. This product is sold as part of our Total Yeast Detox Package or it can be purchased separately. | Not published in this source record | 54 bottles | ***Exp 12/22. Expiration Date: 12/20200 ***Lot #0120011Q. |
Distribution
- distributed in IN
- KY
- MN
- MO
- MT
- NE
- NY
- OH
- PA
- TN
- VA
- and WI and in Ontario of Canada.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0272-2022
- Event ID
- 89066
- Status
- Terminated
- Classification
- Class I
- Company
- Mountain Meadow Herbs, Inc.
- Product description
- Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3, 500 mg per capsule, 240 capsules per bottle. UPC 8 13086 01593 2. This product is sold as part of our Total Yeast Detox Package or it can be purchased separately.
- Quantity
- 54 bottles
- Reason
- Product bottle has potential to become pressurized over time. When consumer opens a bottle, the cap, capsules, and product powder could be forcefully expelled, and customers may sustain injuries to their hands and eyes.
- Recall initiation date
- November 16, 2021
- Report date
- December 15, 2021
- Classification date
- Not published in this source record
- Termination date
- January 11, 2022
- Distribution pattern
- distributed in IN, KY, MN, MO, MT, NE, NY, OH, PA, TN, VA, and WI and in Ontario of Canada.
- UPC, lot, and code information
- ***Exp 12/22. Expiration Date: 12/20200 ***Lot #0120011Q.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Mountain Meadow Herbs, Inc.
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 |
|---|---|
| Indiana | 1 |
| Kentucky | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Montana | 1 |
| Nebraska | 1 |
| New York | 1 |
| Ohio | 1 |
| Pennsylvania | 1 |
| Tennessee | 1 |
| Virginia | 1 |
| Wisconsin | 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.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
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?
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of January 11, 2022.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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.