Alfalfa Sprouts (Rhodes Legacy) – Salmonella risk (2022)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Sun Sprouts Alfalfa Sprouts packaged in 4 oz plastic clamshell, 6/4 oz or 12/4 oz containers per case; Sun Sprouts Alfalfa Sprouts packaged in 2.5lb plastic lined box.
Brand
Rhodes Legacy, Inc.
Lot Codes / Batch Numbers
Lot 4211, Sell by date 12/10/22 through 12/14/22, Lot 5211, Sell by date 12/17/22 through 12/27/22, Lot 3212, Sell by date 12/26/22 through 12/31/22, Lot 4212, Sell by date 1/3/23 through 1/7/23.
Products Sold
Lot 4211, Sell by date 12/10/22 through 12/14/22; Lot 5211, Sell by date 12/17/22 through 12/27/22; Lot 3212, Sell by date 12/26/22 through 12/31/22; Lot 4212; Sell by date 1/3/23 through 1/7/23.
Rhodes Legacy, Inc. is recalling Sun Sprouts Alfalfa Sprouts packaged in 4 oz plastic clamshell, 6/4 oz or 12/4 oz containers per cas due to Alfalfa sprouts have the potential to be contaminated with Salmonella.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Alfalfa sprouts have the potential to be contaminated with Salmonella.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IN, IA, KS, NE
Page updated: Jan 6, 2026