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FDA source record Class II Ongoing

Champagne Wafer - Raspberry Almond [Two sizes: retail package of 8 wafers (7 oz) and retail gift package of 2 wafers (2 oz)]

Recall Date: 2024-04-17 Recalling Firm: Sacramento Cookie Factory Record Ref: F-1217-2024

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Champagne Wafer - Raspberry Almond [Two sizes: retail package of 8 wafers (7 oz) and retail gift package of 2 wafers (2 oz)] and names Sacramento Cookie Factory as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Sacramento Cookie Factory
  • Classification: Class II
  • Status: Ongoing
  • Recall date: 2024-04-17
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Product Description & Identification

Champagne Wafer - Raspberry Almond [Two sizes: retail package of 8 wafers (7 oz) and retail gift package of 2 wafers (2 oz)]

Reason for Recall / Hazard Identified

Undeclared allergen (milk)

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

U.S. Distribution to the following states: CA, AK, IA, NY, TX, FL, WA, NJ, WA, VA, GA, TN, AZ, AL, NC. For foreign or government distribution.

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-1217-2024
Indexed update
2026-08-09 21:59:13 UTC
Official source
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