🔍 RecallPedia

Bunches of curly parsley packed in cardboard cases received at distributor level with following labeling: Herb Parsley Curly Grown in Salinas 60EA x 60EA Bunch US or 30EA x 60EA Bunch US Dole Fresh Vegetables, Monterey, CA 93940 PLU 4899 0 07143 00310 Harvest Date Aug18 Bunches of curly parsley displayed on produce retail shelf tied with binding twist tie with following labeling: Curly Parsley Persil Frise Product of USA #4899 Product Des Etatis-Unis 0 33383 80110 0

Class I - Dangerous
🍎 Food Recalled: September 9, 2021 Dole Fresh Vegetables Produce

What Should You Do?

  1. Check if you have this product:
    PLU #4899
  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:
Dole Fresh Vegetables Inc
Reason for Recall:
Potential non-O157 STEC (Shiga-Toxin 1) contamination. Serotype OXY31:H20 (stx1a with saa)
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Bunches of curly parsley packed in cardboard cases received at distributor level with following labeling: Herb Parsley Curly Grown in Salinas 60EA x 60EA Bunch US or 30EA x 60EA Bunch US Dole Fresh Vegetables, Monterey, CA 93940 PLU 4899 0 07143 00310 Harvest Date Aug18 Bunches of curly parsley displayed on produce retail shelf tied with binding twist tie with following labeling: Curly Parsley Persil Frise Product of USA #4899 Product Des Etatis-Unis 0 33383 80110 0

Product Codes/Lot Numbers:

PLU #4899

Distribution:

Distributed in: FL, IA, MI, MN, MO

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0013-2022

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