Class ITerminated in FDA datasetRecall initiated Feb 19, 2016

Sweetwater Sprouts 100% Pure Sprouted Mung Bean packaged in the following configurations: 8 oz.…

Recalling firm: Sweetwater Farms LLC

Why it was recalled

Sprouts are potentially contaminated with Salmonella

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 1, 2017.

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ProductSweetwater Sprouts 100% Pure Sprouted Mung Bean packaged in the following configurations: 8 oz. plastic bags packed 10 per case; 16 oz. plastic bags packed in cases of 5 or 10; 5 lb. bulk case; 10 lb. bulk case. The product is shipped in cardboard cases labeled with product and lot number. The responsible name on the label is Sweetwater Farms, Inman, KS 67546.
Package size8 oz

FDA code information

lot 039016, sell by 2/22/2016; lot 040016, sell by 2/232016; lot 041016, sell by 2/24/2016; lot 042016, sell by 2/25/2016; lot 043016, sell by 2/26/2016; lot 044016, sell by 2/27/2016; lot 046016, sell by 2/29/2016; lot 047016, sell by 3/1/2016; lot 048016, sell by 3/2/2016; lot 050016, sell by 3/4/2016; lot 051016, sell by 3/5/2016; and lot 053016, sell by 3/7/2016

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Full FDA record and distribution details

Original product description

Sweetwater Sprouts 100% Pure Sprouted Mung Bean packaged in the following configurations: 8 oz. plastic bags packed 10 per case; 16 oz. plastic bags packed in cases of 5 or 10; 5 lb. bulk case; 10 lb. bulk case. The product is shipped in cardboard cases labeled with product and lot number. The responsible name on the label is Sweetwater Farms, Inman, KS 67546.

Original FDA recall reason

Sprouts are potentially contaminated with Salmonella

Recall details

Recall number
F-1033-2016
Event ID
73341
FDA status
Terminated
Initiated
Feb 19, 2016
Reported
Apr 13, 2016
Classified
Apr 5, 2016
Terminated
May 1, 2017
Quantity
3900/ 8oz./bags; 2585/ 16 oz./bags; 454/5 lb./cases; 427/10 lb./cases (11,075 lbs.)
Location
Inman, KS, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Arkansas, Kansas, and Oklahoma

FDA source record · F-1033-2016

Data updated September 16, 2026. View official FDA data ↗

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