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Braga Fresh Foods Recall: Undeclared milk and egg

United States

TerminatedClass I

Company
Braga Fresh Foods
Product
365 by Whole Foods Market Organic Asian Inspired Chopped Sal…
Recall date
July 10, 2023
Terminated
September 17, 2024
Source
FDA

Reason for recall

Undeclared milk and egg

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
365 by Whole Foods Market Organic Asian Inspired Chopped Salad Kits 12 oz plastic bags 9 bags per case UPC: 9948246932 Item#: 9770522 9948246932 673 cases Lot code - BFFS179A2 Best if Used By: 7/16/2023

Distribution

  • Product was distributed to Whole Foods Market
  • and further distributed to 280 retail locations nationwide

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1293-2023
Event ID
92684
Status
Terminated
Classification
Class I
Company
Braga Fresh Foods
Product description
365 by Whole Foods Market Organic Asian Inspired Chopped Salad Kits 12 oz plastic bags 9 bags per case UPC: 9948246932 Item#: 9770522
Quantity
673 cases
Reason
Undeclared milk and egg
Recall initiation date
July 10, 2023
Report date
July 26, 2023
Classification date
Not published in this source record
Termination date
September 17, 2024
Distribution pattern
Product was distributed to Whole Foods Market, and further distributed to 280 retail locations nationwide
UPC, lot, and code information
UPC 9948246932; Lot code - BFFS179A2 Best if Used By: 7/16/2023
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Other
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Braga Fresh Foods

Other recalls from Braga Fresh Foods

FDA Recall United States Terminated Historical recordClass I

Braga Fresh Foods

Product
Wegman's Organics Sweet Kale Chopped Salad Kit, 8oz.
Published
November 8, 2023
Distribution
Nationwide

View recall →

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:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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.