CLASS I Food recall · Reported 8 Nov 2023 · FDA Enforcement Report

Wegman's Organics Sweet Kale Chopped Salad Kit recalled

Braga Fresh Foods is recalling Wegman's Organics Sweet Kale Chopped Salad Kit, distributed nationwide in the US. The recall was initiated on 17 Oct 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot: BFFS282B4; Best By: 10/27/2023; GTIN: 10077890559113

Quantity recalled525 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-0312-2024
FDA event ID: 93164
Recalling firm: Braga Fresh Foods, Salinas, CA
Brand: Wegman's Organics
Classification: Class I
Status: Terminated
Recall initiated: 17 Oct 2023
FDA classified: 1 Nov 2023
Reported: 8 Nov 2023
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Undeclared Egg
Product category: Salad Kits

Timeline

17 Oct 2023	Recall initiated by company
1 Nov 2023	Classified by FDA	+15 days
8 Nov 2023	Published in enforcement report	+7 days

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

Reason for recall

Undeclared egg

Product as listed by the FDA

Wegman's Organics Sweet Kale Chopped Salad Kit, 8oz.

Where it was distributed

Firm distributed nationwide; primary distribution to DCs: VA, PA, NY. Secondary Distribution store locations: NJ, MD, MA, NC, DE, DC

Nationwide District of Columbia Delaware Massachusetts Maryland North Carolina New Jersey New York Pennsylvania Virginia

Questions about this recall

Why was it recalled?

Undeclared egg

Which lots are affected?

Lot: BFFS282B4; Best By: 10/27/2023; GTIN: 10077890559113

Where was it sold?

Firm distributed nationwide; primary distribution to DCs: VA, PA, NY. Secondary Distribution store locations: NJ, MD, MA, NC, DE, DC

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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