CONAGRA BRANDS Recall: potential presence of an extraneous material (plastic)

🇺🇸 United States

1. May 6, 2021 - Recall initiated
2. May 26, 2021 - Reported by source
3. February 15, 2022 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0552-2021

Event ID

87890

Status

Terminated

Classification

Class II

Company

CONAGRA BRANDS

Product description

Udi Gluten Free Chocolate Zucchini Muffins, 10oz retail container of 4 muffins, 6 retail units per wholesale case. Retail unit UPC: 00-6-98997-81014-8

Quantity

816 cases

Reason

potential presence of an extraneous material (plastic)

Recall initiation date

May 6, 2021

Report date

May 26, 2021

Classification date

Not published in this source record

Termination date

February 15, 2022

Distribution pattern

Retailers and distributors nationwide and Canada.

UPC, lot, and code information

UPC 00-6-98997-81014-8; Lot code 1F11071G31 1F25081G31 Best By 11JUL21 25AUG21

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 87890 with 3 other product entries in Public Health Trace.

Responsible company: CONAGRA BRANDS

Other recalls from CONAGRA BRANDS

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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