Sweetwater Sprouts 100% Pure Sprouted Alfalfa packaged in the following configurations: 4 oz. plastic bags (UPC 7 56733 00104 2) packed 12 per case; 16 oz. (1 lb.) plastic bags; and 5 lb. bulk boxes The product is shipped in cardboard cases labeled with product and lot number. The responsible name on the label is Sweetwater Farms LLC, Inman, KS 67456.

Class I - Dangerous
Recalled: February 19, 2016 Sweetwater Farms Beverages

What Should You Do?

  1. Check if you have this product:
    lot 039016, sell by date 2/29/2016; lot 042016, sell by date 3/3/2016; lot 046016, sell by 3/7/2016; and lot 053016, sell by 3/14/2016
  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:
Sweetwater Farms LLC
Reason for Recall:
Sprouts are potentially contaminated with Salmonella
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Sweetwater Sprouts 100% Pure Sprouted Alfalfa packaged in the following configurations: 4 oz. plastic bags (UPC 7 56733 00104 2) packed 12 per case; 16 oz. (1 lb.) plastic bags; and 5 lb. bulk boxes The product is shipped in cardboard cases labeled with product and lot number. The responsible name on the label is Sweetwater Farms LLC, Inman, KS 67456.

Product Codes/Lot Numbers:

lot 039016, sell by date 2/29/2016; lot 042016, sell by date 3/3/2016; lot 046016, sell by 3/7/2016; and lot 053016, sell by 3/14/2016

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1031-2016

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