IMPORTED DRY MUSHROOMS, bulk box 30 lbs, distributed by Kirsch Mushroom Co. Inc., 751 Drake St., Bronx, NY 10474 (labeling for bulk product not provided by NYSDAM) --- Repacked product: IMPORTED DRY MUSHROOMS, WEIGHT XXX - SLOAN SUPERMARKET 494 REIMAN STREET SLOAN, N.Y. 14212 --- The mushrooms were sold in a bulk master box (30 lbs.) and repacked by direct account (Sloan) for retail sales.

Class I - Dangerous
Recalled: February 18, 2015 Kirsch Mushroom Co. Other Foods

What Should You Do?

  1. Check if you have this product:
    Uncoded; purchased from November 1, 2014 to December 20, 2014
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Kirsch Mushroom Co. Inc
Reason for Recall:
The product contained undeclared sulfites (750.4 ppm) based on sampling and analysis by New York State Department of Agriculture & Markets.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

IMPORTED DRY MUSHROOMS, bulk box 30 lbs, distributed by Kirsch Mushroom Co. Inc., 751 Drake St., Bronx, NY 10474 (labeling for bulk product not provided by NYSDAM) --- Repacked product: IMPORTED DRY MUSHROOMS, WEIGHT XXX - SLOAN SUPERMARKET 494 REIMAN STREET SLOAN, N.Y. 14212 --- The mushrooms were sold in a bulk master box (30 lbs.) and repacked by direct account (Sloan) for retail sales.

Product Codes/Lot Numbers:

Uncoded; purchased from November 1, 2014 to December 20, 2014

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1919-2015

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