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Spring Glen Fresh Foods Recall: Undeclared egg and milk due to mis-labeling. - F-0093-2021

United States

TerminatedClass I

Company
Spring Glen Fresh Foods
Product
Rice Pudding 5lb plastic containers. UPC: 4428421260. Refr…
Recall date
October 9, 2020
Terminated
January 13, 2022
Source
FDA

Reason for recall

Undeclared egg and milk due to mis-labeling.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Rice Pudding 5lb plastic containers. UPC: 4428421260. Refrigerated 34¿F-38¿F 4428421260 272 containers Best By: 10-17-20, Best By: 10-23-20; and Best By:10-30-20

Distribution

  • Distributed to distributors in Maryland
  • Pennsylvania
  • and Delaware.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0093-2021
Event ID
86611
Status
Terminated
Classification
Class I
Company
Spring Glen Fresh Foods
Product description
Rice Pudding 5lb plastic containers. UPC: 4428421260. Refrigerated 34¿F-38¿F
Quantity
272 containers
Reason
Undeclared egg and milk due to mis-labeling.
Recall initiation date
October 9, 2020
Report date
November 11, 2020
Classification date
Not published in this source record
Termination date
January 13, 2022
Distribution pattern
Distributed to distributors in Maryland, Pennsylvania, and Delaware.
UPC, lot, and code information
UPC 4428421260; Best By: 10-17-20, Best By: 10-23-20; and Best By:10-30-20
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

Responsible company: Spring Glen Fresh Foods

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 I mean?

FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.

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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of January 13, 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

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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