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High RiskFDAfda-F-1848-2016MISLABELED

Xtra Immunity Brown Rice Antioxidant Probiotic Extract, a liquid packaged in a 500mL bottle. UPC 184368000114. The responsible firm name...

Category
Units Affected
3,940
Recall Date
June 17, 2016
Issuing Agency
Hazard
Mislabeled

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1848-2016.

The product is a dietary supplement with drug claims, making the product misbranded.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1848-2016.

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 Sustainable Community Development Llc Dba Scd Probiotics 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-1848-2016.

Sustainable Community Development LLC dba SCD Probiotics

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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Sustainable Community Development Llc Dba Scd Probiotics Recall FAQ

Sustainable Community Development Llc Dba Scd Probiotics is the subject of a food safety report: Xtra Immunity Brown Rice Antioxidant Probiotic Extract, a liquid packaged in a 500mL bottle. UPC 184368000114. The responsible firm name.... The notice was published on June 17, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 3,940 units are potentially affected.