RecallHawk
Class I Recall

Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3, 500 mg per capsule, 240 capsules per bottle. UPC 8 13086 0

Mountain Meadow Herbs, Inc.

Summary

The FDA issued a Class I for Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3, 500 mg per capsule, by Mountain Meadow Herbs, Inc.. Reason: Product bottle has potential to become pressurized over time. When consumer opens a bottle, the cap, capsules, and product powder could be forcefully.

Details

Source

Food Recall

External ID

F-0272-2022

Action Date

2021-12-15

Status

Terminated

Category

food

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.

Lot/Code Info: ***Exp 12/22. Expiration Date: 12/20200 ***Lot #0120011Q.

Quantity Affected: 54 bottles

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.

Distribution

distributed in IN, KY, MN, MO, MT, NE, NY, OH, PA, TN, VA, and WI and in Ontario of Canada.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-11-16

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 60 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Mountain Meadow Herbs, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Mountain Meadow Herbs, Inc. have FDA actions?

This is the only FDA action we have on record for Mountain Meadow Herbs, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0272-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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