IMPORTED DRY MUSHROOMS, bulk box 30 lbs, distributed by Kirsch Mushroom Co. Inc., 751 Drake St., Bronx, NY 10474 (labeling for bulk produ...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1919-2015.
The product contained undeclared sulfites (750.4 ppm) based on sampling and analysis by New York State Department of Agriculture & Markets.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1919-2015.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Kirsch Mushroom Co. Inc or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- 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-1919-2015.
Kirsch Mushroom Co. Inc
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.
Kirsch Mushroom Co. Inc Recall FAQ
Kirsch Mushroom Co. Inc is the subject of a food safety report: IMPORTED DRY MUSHROOMS, bulk box 30 lbs, distributed by Kirsch Mushroom Co. Inc., 751 Drake St., Bronx, NY 10474 (labeling for bulk produ.... The notice was published on February 18, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 495 units are potentially affected.