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FDA source record Class I Terminated

Recalled Meltaways product is packaged in clear cellophane bags, net wt. 4oz and 8 oz. and has no UPC. The front label is read Mint Meltaways, Cranberry Sweets and more, Coos B...

Recall Date: 2022-12-05 Recalling Firm: Cranberry Sweets & More Inc Record Ref: F-0214-2023

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Recalled Meltaways product is packaged in clear cellophane bags, net wt. 4oz and 8 oz. and has no UPC. The front label is read Mint Meltaways, Cranberry Sweets and more, Coos B... and names Cranberry Sweets & More Inc 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: Cranberry Sweets & More Inc
  • Classification: Class I
  • Status: Terminated
  • Recall date: 2022-12-05
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Product Description & Identification

Recalled Meltaways product is packaged in clear cellophane bags, net wt. 4oz and 8 oz. and has no UPC. The front label is read Mint Meltaways, Cranberry Sweets and more, Coos Bay, OR 97402. The back label is read Heirloom Mint Meltaways, Ingredients: Milk Chocolate (***soy lecithin***), Oregon peppermint oil. Contains the following allergens: Milk, Soy.

Reason for Recall / Hazard Identified

Peanut Butter Meltaway was mis-labeled as Mint Meltaways and peanut is undeclared.

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

Distributed to stores in Oregon and Washington and sold nationwide through direct orders.

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-0214-2023
Indexed update
2026-08-09 21:59:13 UTC
Official source
Open issuing-agency record