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CriticalFDAfda-F-0858-2020E COLI

Red Clover 4 oz, Red Clover 2 Lbs. Products have Red Clover as an ingredient.

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (e coli). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
2
Recall Date
March 12, 2020
Issuing Agency
Hazard
E Coli

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0858-2020.

FDA sample analysis of sprouts was positive for E. coli. FDA traceback and epi associate the firm's sprouts with an outbreak of E. coli.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0858-2020.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Chicago Indoor Garden, Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0858-2020.

Chicago Indoor Garden, Inc.

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Chicago Indoor Garden, Inc. Recall FAQ

Chicago Indoor Garden, Inc. is the subject of a food safety report: Red Clover 4 oz, Red Clover 2 Lbs. Products have Red Clover as an ingredient.. The notice was published on March 12, 2020 by the U.S. Food and Drug Administration (FDA). Approximately 2 units are potentially affected.