Rhodes Legacy, Inc. Recall: Alfalfa sprouts have the potential to be contaminated with Salmonella.
United States
TerminatedClass I
- Company
- Rhodes Legacy, Inc.
- Product
- Sun Sprouts Alfalfa Sprouts packaged in 4 oz plastic clamshe…
- Recall date
- December 28, 2022
- Terminated
- February 9, 2023
- Source
- FDA
Reason for recall
Alfalfa sprouts have the potential to be contaminated with Salmonella.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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. | Not published in this source record | 1406 lbs | 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. |
Distribution
- Sold to distributors and a retailer in Nebraska
- Kansas
- and Iowa.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0290-2023
- Event ID
- 91414
- Status
- Terminated
- Classification
- Class I
- Company
- Rhodes Legacy, Inc.
- Product description
- 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.
- Quantity
- 1406 lbs
- Reason
- Alfalfa sprouts have the potential to be contaminated with Salmonella.
- Recall initiation date
- December 28, 2022
- Report date
- January 25, 2023
- Classification date
- Not published in this source record
- Termination date
- February 9, 2023
- Distribution pattern
- Sold to distributors and a retailer in Nebraska, Kansas, and Iowa.
- UPC, lot, and code information
- 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.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Telephone
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Rhodes Legacy, Inc.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
