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High RiskFDAfda-F-1412-2014UNDECLARED ALLERGEN

Harry & David; WILD 'N SPICY; JALAPENO TOMATO CHEESE DIP; NET WT 1 lb.; (453g);Medium; in glass jars; MADE FOR HARRY AND DAVID, MEDFORD,...

Category
Units Affected
636
Recall Date
February 19, 2014
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1412-2014.

Undeclared Wheat due to a supplier's inadvertent use of a wheat product instead of whey in preparing the cheese premix for the recalling firm.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1412-2014.

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 Fischer & Wieser Specialty Foods 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-1412-2014.

Fischer & Wieser Specialty Foods

FDA

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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 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.

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Fischer & Wieser Specialty Foods Recall FAQ

Fischer & Wieser Specialty Foods is the subject of a dairy safety report: Harry & David; WILD 'N SPICY; JALAPENO TOMATO CHEESE DIP; NET WT 1 lb.; (453g);Medium; in glass jars; MADE FOR HARRY AND DAVID, MEDFORD,.... The notice was published on February 19, 2014 by the U.S. Food and Drug Administration (FDA). Approximately 636 units are potentially affected.