Onions Peeled. Products are labeled in part: "***Onions ***Yellow Whole Peeled***Read To Eat Product***4/5 LB***". "***FP CENTRAL FL. FRESHCUTS ONIONS, FC YELLOW COLOSSAL PEELED***4/5#***RT # FC***" Item # 515670 ONIONS, FC YELLOW COLOSSAL PEELED 4/5#; Item # 514003 ONIONS, FC YELLOW WHOLE PEELED FC 4/5#; Item # 480142 ONIONS, FC YELLOW WHOLE PLD UNIVER 1 1/5# Item # 514035 ONIONS, FC YELLOW WHOLE PEELED 2/10#.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Item #: 515670; 514003; 514035 ; 480142.
- 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:
- FreshPoint Central Florida
- Reason for Recall:
- FreshPoint Central Florida is recalling multiple onion products and mixes. The products were prepared using onions sourced from Gills Onions LLC which may be adulterated with Listeria monocytogenes.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Onions Peeled. Products are labeled in part: "***Onions ***Yellow Whole Peeled***Read To Eat Product***4/5 LB***". "***FP CENTRAL FL. FRESHCUTS ONIONS, FC YELLOW COLOSSAL PEELED***4/5#***RT # FC***" Item # 515670 ONIONS, FC YELLOW COLOSSAL PEELED 4/5#; Item # 514003 ONIONS, FC YELLOW WHOLE PEELED FC 4/5#; Item # 480142 ONIONS, FC YELLOW WHOLE PLD UNIVER 1 1/5# Item # 514035 ONIONS, FC YELLOW WHOLE PEELED 2/10#.
Product Codes/Lot Numbers:
Item #: 515670; 514003; 514035 ; 480142.
Distribution:
Distributed in: FL
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-1869-2012
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