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CriticalFDAfda-F-2536-2016E COLI

The Inebriated Apple Wine Brownie Mix, packaged in a plastic bag which is placed in a cardboard box, net wt. 11oz, UPC 010749040151

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (e coli). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
30
Recall Date
August 9, 2016
Issuing Agency
Hazard
E Coli

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2536-2016.

Bread, muffin, and brownie mixes may have been manufactured with flour contaminated with E. coli O121

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2536-2016.

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 Rabbit Creek Products Inc. 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-2536-2016.

Rabbit Creek Products Inc.

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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Rabbit Creek Products Inc. Recall FAQ

Rabbit Creek Products Inc. is the subject of a food safety report: The Inebriated Apple Wine Brownie Mix, packaged in a plastic bag which is placed in a cardboard box, net wt. 11oz, UPC 010749040151. The notice was published on August 9, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 30 units are potentially affected.