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CriticalFDAfda-F-1675-2012UNDECLARED ALLERGEN

Crispy by TWI Foods Almond Cake Rusk, Biscotte Croustillante Almande, Net Wt 750 g, Product of Canada Manufactured by TWI Foods Inc. 186...

⚠ 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.

Units Affected
72
Recall Date
April 17, 2012
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1675-2012.

Product may contain undeclared milk.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1675-2012.

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 Indian Foods & Spices, Llc 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-1675-2012.

Indian Foods & Spices, LLC

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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Indian Foods & Spices, Llc Recall FAQ

Indian Foods & Spices, Llc is the subject of a bakery & grains safety report: Crispy by TWI Foods Almond Cake Rusk, Biscotte Croustillante Almande, Net Wt 750 g, Product of Canada Manufactured by TWI Foods Inc. 186.... The notice was published on April 17, 2012 by the U.S. Food and Drug Administration (FDA). Approximately 72 units are potentially affected.