Kellogg's Variety and Assortment Packs containing Frosted/ Unfrosted Mini Wheats, Bite Size, Lightly Sweetened Whole Grain Wheat Cereal, 10 ct; 30 ct, 72 ct , 96 ct.
Class I - DangerousWhat Should You Do?
- Check if you have this product: USA ONLY products with the letters FK, HG preceding or following the Better If Used Before Date Apr 01 2013 - Sep 21 2013. Case UPC: 3800005337, 3800070418, 3800022055, 3800038118, 3800007337, 3800007338. Carton UPC3800005332, 3800070973, 3800022056, 3800038118, 3800007337, 3800007338
- 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:
- Kellogg Company
- Reason for Recall:
- This voluntary recall is initiated due to the possible presence of fragments of flexible metal mesh from a faulty manufacturing part that were found in certain Mini-WheatsÂż cereal produced in a single Kellogg plant between April 1 and September 21, 2012.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Kellogg's Variety and Assortment Packs containing Frosted/ Unfrosted Mini Wheats, Bite Size, Lightly Sweetened Whole Grain Wheat Cereal, 10 ct; 30 ct, 72 ct , 96 ct.
Product Codes/Lot Numbers:
USA ONLY products with the letters FK, HG preceding or following the Better If Used Before Date Apr 01 2013 - Sep 21 2013. Case UPC: 3800005337, 3800070418, 3800022055, 3800038118, 3800007337, 3800007338. Carton UPC3800005332, 3800070973, 3800022056, 3800038118, 3800007337, 3800007338
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-0602-3013
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