Everything Sprouts, LLC Expands Voluntarily Recall to Include Robust Radish Mix Due to Potential E. Coli and Salmonella Risk
United States
Status not reported
- Product
- Everything Sprouts, LLC Expands Voluntarily Recall to Includ…
- Source
- FDA
Reason for recall
Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Everything Sprouts, LLC Expands Voluntarily Recall to Include Robust Radish Mix Due to Potential E. Coli and Salmonella Risk | Not published in this source record | Not published in this source record | Not published in this source record |
Distribution area was not published in this source record.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Safety Recalls (RSS)
- Recall number
- http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/everything-sprouts-llc-expands-voluntarily-recall-include-robust-radish-mix-due-potential-e-coli-and
- Status
- Not published in this source record
- Classification
- Not yet classified
- Company
- Not published in this source record
- Product description
- Everything Sprouts, LLC Expands Voluntarily Recall to Include Robust Radish Mix Due to Potential E. Coli and Salmonella Risk
- Quantity
- Not published in this source record
- Reason
- Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.
- Recall initiation date
- Not published in this source record
- Report date
- August 28, 2026
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- Not published in this source record
- UPC, lot, and code information
- Not published in this source record
- Voluntary or mandated
- Not published in this source record
- Initial notification method
- Not published in this source record
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Where this information comes from
View public notice -- the original notice published by FDA.
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 recall classification mean?
The agency has not yet assigned a recall classification.
Is this recall still active?
According to FDA, this recall's status is "not yet published." 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.
