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CriticalFDAfda-F-2249-2017CONTAMINATION

Herbal Tea Variety 120 ml/pouch, 40 pouches/case

⚠ Critical Alert — Stop Using Immediately

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

Category
Units Affected
9,480
Recall Date
May 2, 2017
Issuing Agency
Hazard
Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2249-2017.

US Deer Antler Export and Import is recalling a variety of Herbal Teas because they may be contaminated with Clostridium botulinum

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2249-2017.

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 U S Deer Antlers Export & Import 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-2249-2017.

U S Deer Antlers Export & Import

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.

How to report to FDAFile a report at FDA

U S Deer Antlers Export & Import Recall FAQ

U S Deer Antlers Export & Import is the subject of a beverages safety report: Herbal Tea Variety 120 ml/pouch, 40 pouches/case. The notice was published on May 2, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 9,480 units are potentially affected.