Product labeled "Herb Roasted Potatoes", packed in 16oz plastic tray with clear plastic shrink-wrapping. Product is visible through clea...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1389-2019.
Mislabeling and Undeclared allergens: Baked Potatoes with Cheddar Cheese & Bacon were mislabeled as Herb Roasted Potatoes.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1389-2019.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Ukrop's Homestyle Foods, Llc or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1389-2019.
Ukrop's Homestyle Foods, LLC
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Ukrop's Homestyle Foods, Llc Recall FAQ
Ukrop's Homestyle Foods, Llc is the subject of a dairy safety report: Product labeled "Herb Roasted Potatoes", packed in 16oz plastic tray with clear plastic shrink-wrapping. Product is visible through clea.... The notice was published on November 6, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 78 units are potentially affected.