Fresh Recalls

FDAClass II · Food · Recall H-1245-2026 · Recalled August 26, 2026

Gifford's HomeMaine ice cream brand POWER PLAY FUDGE recall — Gifford's Dairy, Inc.

Agency report date: August 26, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Gifford's HomeMaine ice cream brand POWER PLAY FUDGE
Company / brand
Gifford's Dairy
Lot / serial / date codes
Lot Code: 26184. Best By date: 08/27/27.
Distribution
MA, ME, VT
Agency product description and boundaries

Gifford's HomeMaine ice cream brand POWER PLAY FUDGE; ONE QUART (946 mL); UPC: 8 60864 00030 7

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Potential foreign object contamination: rubber pieces

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Gifford's HomeMaine ice cream brand POWER PLAY FUDGE recall status

3. Open the official notice or contact

Official recall ID
H-1245-2026
Brand
All Gifford's Dairy recalls
Classification
Class II
Units affected
3,585 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Skowhegan, ME, United States
Firm address
25 Hathaway St, 04976-1436

Identifying details (verbatim from the notice)

Product codes / lots
Lot Code: 26184. Best By date: 08/27/27.
Distribution
MA, ME, VT
Firm notified the public via
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID
99663
Recall initiated
August 14, 2026
FDA classified
August 19, 2026
FDA report date
August 26, 2026

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 12:00 PM UTC. Record retrieved October 22, 2026 at 12:00 PM UTC.

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