Skip to main content
RecallFDAfda-F-0907-2020UNDECLARED ALLERGEN

DION DION DRIED MUSHROOMS, Product Origin from Haiti, Net Wt. 1/4 oz

Category
Units Affected
25
Recall Date
February 27, 2020
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0907-2020.

Undeclared sulfites in product label.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0907-2020.

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 Dana Usa Corp. 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-0907-2020.

DANA USA Corp.

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.

Visit FDA.gov →

📣 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

Dana Usa Corp. Recall FAQ

Dana Usa Corp. is the subject of a food safety report: DION DION DRIED MUSHROOMS, Product Origin from Haiti, Net Wt. 1/4 oz. The notice was published on February 27, 2020 by the U.S. Food and Drug Administration (FDA). Approximately 25 units are potentially affected.