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 - DangerousWhat Should You Do?
- Check if you have this product: PLU #4899
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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.govFDA Recall Number: F-0013-2022
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