FDA recall record

Brew Dr recall — FDA F-1619-2018

Brew Dr. Kombucha US Clear Mind, 32 oz bottles, is recalled because glass fragments were found inside the bottle.

Class IIclassification
F-1619-2018official record ID
Jul 18, 2018report date

Recall record at a glance

Official recordF-1619-2018
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBrew Dr Kombucha, LLC
Report dateJul 18, 2018
Recall initiation dateJun 22, 2018
Quantity3,150 bottles (525 cases)
LocationPortland, OR, United States

Official 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 ***".

Why the product was recalled

Brew Dr. Kombucha US Clear Mind, 32 oz bottles, is recalled because glass fragments were found inside the bottle.

Distribution information

distributed in CA, CO, NY, OR, WA, and WI.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.