CLASS II ONGOING Food recall · Reported 26 Aug 2026 · FDA Enforcement Report
Gifford's HomeMaine ice cream Power Play Fudge recalled
Gifford's Dairy is recalling Gifford's HomeMaine ice cream Power Play Fudge, distributed in Massachusetts, Maine, Vermont. The recall was initiated on 14 Aug 2026 and the FDA has classified it as Class II.
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
- H-1245-2026
- FDA event ID
- 99663
- Recalling firm
- Gifford's Dairy, Skowhegan, ME
- Brand
- Gifford's HomeMaine
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 14 Aug 2026
- FDA classified
- 19 Aug 2026
- Reported
- 26 Aug 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Foreign Material
- Product category
- Ice Cream & Frozen Desserts
Timeline
| 14 Aug 2026 | Recall initiated by company | |
| 19 Aug 2026 | Classified by FDA | +5 days |
| 26 Aug 2026 | 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
Potential foreign object contamination: rubber pieces
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
Gifford's HomeMaine ice cream brand POWER PLAY FUDGE; ONE QUART (946 mL); UPC: 8 60864 00030 7
Where it was distributed
MA, ME, VT
Questions about this recall
Why was it recalled?
Potential foreign object contamination: rubber pieces
Which lots are affected?
Lot Code: 26184. Best By date: 08/27/27.
Where was it sold?
MA, ME, VT
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
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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