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Lower risk Food recall · FDA · Published June 22, 2018

Brew Dr Kombucha Clear Mind Bottles Recall: Glass Fragments Found

Brew Dr Kombucha recalls 32oz Clear Mind bottles with glass fragments. Consumers should check labels for UPC 51107 and lot code P848. No remedy specified in recall notice.

🇺🇸 FDA recall #F-1619-2018FoodBrew Dr Kombucha ›
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Contact the company

Recalling firmBrew Dr Kombucha, LLC4245 SE Milwaukie Ave · Portland, OR 97202-3958
✎ GovInfoNow plain-language explainer

Brew Dr Kombucha is recalling 32-ounce Clear Mind bottles that contain glass fragments. This hazard could cause injury if the bottle breaks during use. Read more at govinfonow.com/recall/19022-brew-dr-kombucha-clear-mind-bottles-recall-glass-fragments-found.

Source Summary by GovInfoNow · govinfonow.com/recall/19022-brew-dr-kombucha-clear-mind-bottles-recall-glass-fragments-found · Updated October 6, 2026 · FDA enforcement record: FDA #F-1619-2018

Cite this page

“Brew Dr Kombucha Clear Mind Bottles Recall: Glass Fragments Found.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/19022-brew-dr-kombucha-clear-mind-bottles-recall-glass-fragments-found. Based on FDA recall #F-1619-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1619-2018%22&limit=1).

The FDA announced on June 22, 2018, that Brew Dr Kombucha LLC voluntarily recalled Brew Dr. Kombucha Clear Mind due to glass fragments found inside the bottles. The agency classified this Class II recall.

How to tell if you have it

  • Brand: Brew Dr Kombucha
  • Product: Brew Dr. Kombucha Clear Mind
  • Item Code: FCG0002
  • UPC: 5110700369
  • Lot Code: P848
  • Best By Dates: 1/02/19, 1/03/19
  • Size: 32 FL OZ (946 ML)
  • Distribution: CA, CO, NY, OR, WA, and WI

The hazard

The recall is necessary because glass fragments were found inside the Brew Dr. Kombucha Clear Mind 32 oz bottles, according to the FDA.

Context

GovInfoNow's records show Brew Dr Kombucha LLC has one other recall on record since April 26, 2021, involving yeast contamination in 16oz cans of its Uplift Drink. Other recent recalls of similar products include Lactalis Canada Vanilla Creme Brulee (April 14, 2026), Alain Milliat Orange Marmalade (March 26, 2026), and Dreyer's Grand Outshine Fruit Bars Tangerine (August 18, 2026).

How to tell if you have this one

Check for the label that says 'CLEAR MIND' with ingredients including organic tea and kombucha culture. Look for UPC 51107 and lot code P848 on the bottle.

  • Brand
    Brew Dr Kombucha
  • Product
    Brew Dr Kombucha, LLC recalls Brew Dr. Kombucha Clear Mind, item Code: FCG0002, 6 glass bottles per case, net volume: 32 FL OZ (946 ML). UPC: 51107
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the label with 'CLEAR MIND' and ingredients including organic tea and kombucha culture.

Where it went and when

Where it was distributed

Distributed in 6 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: yesWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: yesCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “distributed in CA, CO, NY, OR, WA, and WI.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Colorado, New York, Oregon, Washington, Wisconsin.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Jun 22, 201812. FDA classified it Class II: Jul 11, 201823. Published in FDA’s Enforcement Report: Jul 18, 201834. FDA terminated the recall: Sep 18, 201842018
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1619-2018 (June 22, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1619-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA