Kombucha Clear Mind (Brew Dr) – Glass Fragment Risk (2018)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
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
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 ***".
Brand
Brew Dr Kombucha, LLC
Lot Codes / Batch Numbers
Lot Code: P848 Best By Dates: 1/02/19, 1/03/19
Products Sold
Lot Code: P848 Best By Dates: 1/02/19, 1/03/19
Brew Dr Kombucha, LLC is recalling Brew Dr. Kombucha Clear Mind, item Code: FCG0002, 6 glass bottles per case, net volume: 32 FL OZ (94 due to Brew Dr. Kombucha US Clear Mind, 32 oz bottles, is recalled because glass fragments were found inside the bottle.. 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
Brew Dr. Kombucha US Clear Mind, 32 oz bottles, is recalled because glass fragments were found inside the bottle.
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
CA, CO, IN, NY, OR, WA, WI
Page updated: Jan 6, 2026