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 ***".
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot Code: P848 Best By Dates: 1/02/19, 1/03/19
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Brew Dr Kombucha, LLC
- Reason for Recall:
- Brew Dr. Kombucha US Clear Mind, 32 oz bottles, is recalled because glass fragments were found inside the bottle.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full 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 ***".
Product Codes/Lot Numbers:
Lot Code: P848 Best By Dates: 1/02/19, 1/03/19
Distribution:
Distributed in: CA, CO, NY, OR, WA, WI
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-1619-2018
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