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CONAGRA BRANDS Recall: potential presence of an extraneous material (plastic) - F-0553-2021

United States

TerminatedClass II

Company
CONAGRA BRANDS
Product
Udi Gluten Free Blueberry Muffins, 10oz (284g) retail contai…
Recall date
May 6, 2021
Terminated
February 15, 2022
Source
FDA

Reason for recall

potential presence of an extraneous material (plastic)

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Udi Gluten Free Blueberry Muffins, 10oz (284g) retail container of 4 muffins, 6 retail units per wholesale case. Retail unit UPC: 00-6-98997-81038-4 (domestic) 00-6-98997-81044-5 (Canada) 00-6-98997-81038-4 24,399 cases Lot code 1F17071G31 1F18071G31 1F19091G31 1F20091G31 1F21081G31 1F22081G31 1F23081G31 Best By 17JUL21 18JUL21 19SEP21 20SEP21 21AUG21 22AUG21 23AUG21

Distribution

  • Retailers and distributors nationwide and Canada.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0553-2021
Event ID
87890
Status
Terminated
Classification
Class II
Company
CONAGRA BRANDS
Product description
Udi Gluten Free Blueberry Muffins, 10oz (284g) retail container of 4 muffins, 6 retail units per wholesale case. Retail unit UPC: 00-6-98997-81038-4 (domestic) 00-6-98997-81044-5 (Canada)
Quantity
24,399 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 00-6-98997-81038-4; Lot code 1F17071G31 1F18071G31 1F19091G31 1F20091G31 1F21081G31 1F22081G31 1F23081G31 Best By 17JUL21 18JUL21 19SEP21 20SEP21 21AUG21 22AUG21 23AUG21
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

Other products recalled under this same event

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

FDA Recall United States TerminatedTerminated: February 15, 2022Historical recordClass II

CONAGRA BRANDS

Product
Udi Gluten Free Double Chocolate Muffins, 10oz (284g) retail…
Published
May 26, 2021
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: February 15, 2022Historical recordClass II

CONAGRA BRANDS

Product
Udi Gluten Free Chocolate Zucchini Muffins, 10oz retail cont…
Published
May 26, 2021
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: February 15, 2022Historical recordClass II

CONAGRA BRANDS

Product
Udi Gluten Free Banana Chocolate Chip Muffins, 10oz retail c…
Published
May 26, 2021
Distribution
Nationwide

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Responsible company: CONAGRA BRANDS

Other recalls from CONAGRA BRANDS

FDA Recall United States TerminatedTerminated: February 7, 2024Historical recordClass I

CONAGRA BRANDS

Product
Wishbone Chunky Blue Cheese Dressing 24oz. bottle UPC 0-4132…
Published
February 16, 2022
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: February 7, 2024Historical recordClass I

CONAGRA BRANDS

Product
Wishbone Thousand Island Dressing 15oz. bottle UPC 0-41321-0…
Published
February 16, 2022
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: January 31, 2023Historical recordClass II

CONAGRA BRANDS

Product
Birds Eye Broccoli Tots, frozen, 12OZ bag UPC 00-0-14500-001…
Published
December 15, 2021
Distribution
Nationwide

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Where this information comes from

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

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

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

Retrieved by Public Health Trace:

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?

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Official guidance and record verification

Public Health Trace does not provide medical advice. The information below explains how to interpret this record and links to relevant official government sources. Review the linked official source for the current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of February 15, 2022.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

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