PlainRecalls
FDA Food Moderate Class II Terminated

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 ***".

Reported: July 18, 2018 Initiated: June 22, 2018 #F-1619-2018

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.

Details

Recalling Firm
Brew Dr Kombucha, LLC
Units Affected
3,150 bottles (525 cases)
Distribution
distributed in CA, CO, NY, OR, WA, and WI.
Location
Portland, OR

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.

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