CLASS I Food recall · Reported 4 Oct 2023 · FDA Enforcement Report

Weis Quality Brownie Moose Tracks Ice Cream recalled

Weis Markets, Inc., Ice Cream Division is recalling Weis Quality Brownie Moose Tracks Ice Cream, distributed in 7 states. The recall was initiated on 30 Aug 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesAll lots

Quantity recalledtotal = 1814 containers & 2045 cases

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-1617-2023
FDA event ID: 92972
Recalling firm: Weis Markets, Inc., Ice Cream Division, Sunbury, PA
Brand: Weis Quality
Classification: Class I
Status: Terminated
Recall initiated: 30 Aug 2023
FDA classified: 28 Sep 2023
Reported: 4 Oct 2023
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Undeclared Egg
Product category: Ice Cream & Frozen Desserts

Timeline

30 Aug 2023	Recall initiated by company
28 Sep 2023	Classified by FDA	+29 days
4 Oct 2023	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared egg

Product as listed by the FDA

Weis Quality Brownie Moose Tracks Ice Cream (48oz)UPC of 041497-01194 Packaged in a scround container. 6 units per case.

Where it was distributed

Retail locations in the following states: DE, MD, NJ, NY, PA, VA, WV

Delaware Maryland New Jersey New York Pennsylvania Virginia West Virginia

Questions about this recall

Why was it recalled?

Undeclared egg

Which lots are affected?

All lots

Where was it sold?

Retail locations in the following states: DE, MD, NJ, NY, PA, VA, WV

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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