CLASS I Food recall · Reported 26 Jul 2023 · FDA Enforcement Report

365 by Whole Foods Market Organic Asian Inspired Chopped Salad Kits recalled

Braga Fresh Foods is recalling 365 by Whole Foods Market Organic Asian Inspired Chopped Salad Kits, distributed nationwide in the US. The recall was initiated on 10 Jul 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot code - BFFS179A2 Best if Used By: 7/16/2023
Quantity recalled673 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1293-2023
FDA event ID
92684
Recalling firm
Braga Fresh Foods, Salinas, CA
Classification
Class I
Status
Terminated
Recall initiated
10 Jul 2023
FDA classified
25 Jul 2023
Reported
26 Jul 2023
Type
Voluntary: Firm initiated
Customers notified by
Other
Reason category
Undeclared Milk
Product category
Salad Kits

Timeline

10 Jul 2023Recall initiated by company
25 Jul 2023Classified by FDA+15 days
26 Jul 2023Published in enforcement report+1 day

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared milk and egg

Product as listed by the FDA

365 by Whole Foods Market Organic Asian Inspired Chopped Salad Kits 12 oz plastic bags 9 bags per case UPC: 9948246932 Item#: 9770522

Where it was distributed

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

Nationwide

Stores named: Whole Foods

Questions about this recall

Why was it recalled?

Undeclared milk and egg

Which lots are affected?

Lot code - BFFS179A2 Best if Used By: 7/16/2023

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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