RecallHawk
Class II Recall

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

Gifford's Dairy, Inc.

Summary

The FDA issued a Class II for Gifford's HomeMaine ice cream brand POWER PLAY FUDGE; ONE QUART (946 mL); UPC: 8 by Gifford's Dairy, Inc.. Reason: Potential foreign object contamination: rubber pieces.

Details

Source

Food Recall

External ID

H-1245-2026

Action Date

2026-08-26

Status

Ongoing

Category

food

Product Description

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

Lot/Code Info: Lot Code: 26184. Best By date: 08/27/27.

Quantity Affected: 3,585 units

Reason for Recall

Potential foreign object contamination: rubber pieces

Distribution

MA, ME, VT

Type: Voluntary: Firm initiated

Recall Initiated: 2026-08-14

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 53 food recalls issued in the same week, part of 82 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Gifford's Dairy, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Gifford's Dairy, Inc. have FDA actions?

This is the only FDA action we have on record for Gifford's Dairy, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1245-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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