Candida Flush (Mountain Meadow Herbs) – pressurization risk (2021)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
Mountain Meadow Herbs, Inc.
Lot Codes / Batch Numbers
***Exp 12/22. Expiration Date: 12/20200 ***Lot #0120011Q.
Products Sold
***Exp 12/22. Expiration Date: 12/20200 ***Lot #0120011Q.
Mountain Meadow Herbs, Inc. is recalling Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3, 500 mg per capsule, 240 capsules per bo due to Product bottle has potential to become pressurized over time. When consumer opens a bottle, the cap, capsules, and product powder could be forcefully. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IN, KY, MN, MO, MT, NE, NY, OH, PA, TN, VA, WI
Page updated: Jan 6, 2026