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CriticalFDAfda-F-0678-2019SALMONELLA CONTAMINATION

Organic Cardamom Green Whole. Product of Guatemala. Product is labeled with a paper label son onto each 25-kg poly-lined, poly-weave "d...

⚠ Critical Alert — Stop Using Immediately

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

Category
Units Affected
2,723
Recall Date
November 6, 2018
Issuing Agency
Hazard
Salmonella Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0678-2019.

Product may be contaminated with Salmonella.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0678-2019.

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 New Forest Llc 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-0678-2019.

NEW FOREST LLC

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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New Forest Llc Recall FAQ

New Forest Llc is the subject of a food safety report: Organic Cardamom Green Whole. Product of Guatemala. Product is labeled with a paper label son onto each 25-kg poly-lined, poly-weave "d.... The notice was published on November 6, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 2,723 units are potentially affected.