CLASS I Food recall · Reported 11 Jan 2023 · FDA Enforcement Report
Meltaways product recalled by Cranberry Sweets & More
Cranberry Sweets & More is recalling Meltaways product is, distributed nationwide in the US. The recall was initiated on 5 Dec 2022 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0214-2023
- FDA event ID
- 91277
- Recalling firm
- Cranberry Sweets & More, Coos Bay, OR
- Brand
- Meltaways
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 5 Dec 2022
- FDA classified
- 4 Jan 2023
- Reported
- 11 Jan 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Undeclared Peanuts
- Product category
- Milk
Timeline
| 5 Dec 2022 | Recall initiated by company | |
| 4 Jan 2023 | Classified by FDA | +30 days |
| 11 Jan 2023 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Peanut Butter Meltaway was mis-labeled as Mint Meltaways and peanut is undeclared.
Product as listed by the FDA
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.
Where it was distributed
Distributed to stores in Oregon and Washington and sold nationwide through direct orders.
Questions about this recall
Why was it recalled?
Peanut Butter Meltaway was mis-labeled as Mint Meltaways and peanut is undeclared.
Which lots are affected?
Code: 032123
Where was it sold?
Distributed to stores in Oregon and Washington and sold nationwide through direct orders.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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