Skip to main content
High RiskFDAfda-F-0098-2015OTHER

Rancheros, sold under brand Heather's Choice. The product is labeled in parts: "***Rancheros***HEATHER'S CHOICE***meals for adventuri...

Category
Units Affected
12
Recall Date
October 1, 2014
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0098-2015.

Heather's Choice Rancheros is being recalled because the firm operated without a permit and lack a HACCP plan.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0098-2015.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Heather's Choice or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. 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-0098-2015.

Heather's Choice

FDA

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.

How to report to FDAFile a report at FDA

Heather's Choice Recall FAQ

Heather's Choice is the subject of a beverages safety report: Rancheros, sold under brand Heather's Choice. The product is labeled in parts: "***Rancheros***HEATHER'S CHOICE***meals for adventuri.... The notice was published on October 1, 2014 by the U.S. Food and Drug Administration (FDA). Approximately 12 units are potentially affected.