Weis Markets, Inc., Ice Cream Division Recall: Undeclared soy and coconut

🇺🇸 United States

1. November 23, 2022 - Recall initiated
2. December 14, 2022 - Reported by source
3. July 10, 2023 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0190-2023

Event ID

91203

Status

Terminated

Classification

Class II

Company

Weis Markets, Inc., Ice Cream Division

Product description

Weis Quality Premium Ice Cream Sea Salt Caramel Ripple 1.5 Quart (1.42 L) UPC 041497-01288

Quantity

108 containers

Reason

Undeclared soy and coconut

Recall initiation date

November 23, 2022

Report date

December 14, 2022

Classification date

Not published in this source record

Termination date

July 10, 2023

Distribution pattern

Distributed to retail stores in Pennsylvania, Maryland, Virginia, New Jersey, New York, Delaware and West Virginia.

UPC, lot, and code information

UPC 041497-01288; Sell by date: 11/08/23

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Weis Markets, Inc., Ice Cream Division

Other recalls from Weis Markets, Inc., Ice Cream Division

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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