Mountain Meadow Herbs, Inc.

FDA Regulatory Profile

Mountain Meadow Herbs, Inc. has 1 FDA recall (1 Class I), 8 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest recall
F-0272-2022 · Class I · Nov 16, 2021
Latest inspection
May 14, 2025 · NAI

Reviewing Mountain Meadow Herbs, Inc. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Mountain Meadow Herbs, Inc. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

Is this your company or a supplier you list? Link to this FDA record from your site with a free button.

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls1 (1 Class I)Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections8Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
F-0272-2022Class IMountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3, 500 mg per capsule, 240 capsules per…Nov 16, 2021

Recent FDA Inspections

DateSiteProductClassificationFEI
May 14, 2025Somers, MTFood/CosmeticsNo Action Indicated (NAI)3004154685
Dec 8, 2021Somers, MTFood/CosmeticsVoluntary Action Indicated (VAI)3004154685
Mar 27, 2019Somers, MTFood/CosmeticsNo Action Indicated (NAI)3004154685
Mar 16, 2016Somers, MTFood/CosmeticsVoluntary Action Indicated (VAI)3004154685
Mar 20, 2015Somers, MTFood/CosmeticsVoluntary Action Indicated (VAI)3004154685
Dec 15, 2011Somers, MTFood/CosmeticsNo Action Indicated (NAI)3004154685
Aug 4, 2010Somers, MTFood/CosmeticsVoluntary Action Indicated (VAI)3004154685
May 15, 2009Somers, MTFood/CosmeticsOfficial Action Indicated (OAI)3004154685

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3004154685Somers, MT8May 14, 2025

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.