Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported July 18, 2018
Brew Dr. Kombucha Clear Mind, item Code: FCG0002, 6 glass bottles per case, net volume: 32 FL OZ (946 ML). UPC: 51107 00369. The bottle's label is read in parts: "***CLEAR MIND***INGREDIENTS: Brewed tea (filtered water, organic green tea, organic rosemary, organic peppermint, organic sage, organic dandelion root), organic cane sugar, live kombucha culture (yeast, bacteria) *** KEEP REFRIGERATED and DO NOT SHAKE ***".
Brew Dr. Kombucha US Clear Mind, 32 oz bottles, is recalled because glass fragments were found inside the bottle.
Brew Dr Kombucha, LLC recalled Brew Dr. Kombucha Clear Mind, item Code: FCG0002, 6 glass bottles per case, net volume: 3… - a moderate-severity action.
Brew Dr. Kombucha Clear Mind, item Code: FCG0002, 6 glass bottles per case, net volume: 3… was recalled by Brew Dr Kombucha, LLC in July 18, 2018. Reason: Brew Dr. Kombucha US Clear Mind, 32 oz bottles, is recalled because glass fragments were found inside the bot…. Check the official notice for the remedy. Verify recall #F-1619-2018 with the FDA Food before acting.
The recall
Brew Dr Kombucha, LLC issued this moderate-severity FDA Food recall-Brew Dr. Kombucha US Clear Mind, 32 oz bottles, is recalled because glass fragments were found inside the bot….
- Moderate
- severity level
- Class II
- classification
- July 18, 2018
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1619-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1619-2018) was formally reported on July 18, 2018, with the manufacturer initiating the action on June 22, 2018. It is classified under Moderate severity (Class II), with a current status of Terminated. Brew Dr Kombucha, LLC is listed as the recalling firm, operating out of Portland, OR. Federal records list the affected scope as 3,150 bottles (525 cases).
The documented reason for this recall is: Brew Dr. Kombucha US Clear Mind, 32 oz bottles, is recalled because glass fragments were found inside the bottle. Distribution data in the federal record shows the product reached: distributed in CA, CO, NY, OR, WA, and WI.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
3,150 bottles (525 cases)
Related Recalls
6
0 from same agency
Product description
Brew Dr. Kombucha Clear Mind, item Code: FCG0002, 6 glass bottles per case, net volume: 32 FL OZ (946 ML). UPC: 51107 00369. The bottle's label is read in parts: "***CLEAR MIND***INGREDIENTS: Brewed tea (filtered water, organic green tea, organic rosemary, organic peppermint, organic sage, organic dandelion root), organic cane sugar, live kombucha culture (yeast, bacteria) *** KEEP REFRIGERATED and DO NOT SHAKE ***".
Reason for recall
Brew Dr. Kombucha US Clear Mind, 32 oz bottles, is recalled because glass fragments were found inside the bottle.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1619-2018 |
| Date reported | July 18, 2018 |
| Date initiated | June 22, 2018 |
| Recalling firm | Brew Dr Kombucha, LLC |
| Firm location | Portland, OR |
| Affected scope | 3,150 bottles (525 cases) |
| Distribution | distributed in CA, CO, NY, OR, WA, and WI. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-1619-2018) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Brew Dr. Kombucha Clear Mind, item Code: FCG0002, 6 glass bottles per case, net volume: 32 FL OZ (946 ML). UPC: 51107 00369. The bottle's label is read in parts: "***CLEAR MIND***INGREDIENTS: Brewed tea (filtered water, organic green tea, organic rosemary, organic peppermint, organic sage, organic dandelion root), organic cane sugar, live kombucha culture (yeast, bacteria) *** KEEP REFRIGERATED and DO NOT SHAKE ***".. Recalled by Brew Dr Kombucha, LLC. Units affected: 3,150 bottles (525 cases).
Why was this product recalled? ▼
Brew Dr. Kombucha US Clear Mind, 32 oz bottles, is recalled because glass fragments were found inside the bottle.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on July 18, 2018. Severity: Moderate. Recall number: F-1619-2018.
Where was the recalled product distributed? ▼
Distribution: distributed in CA, CO, NY, OR, WA, and WI..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1619-2018) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported July 18, 2018. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.