CLASS I Food recall · Reported 22 Feb 2023 · FDA Enforcement Report

Wegmans Asian Chop Salad Kit recalled by Taylor Farms Maryland

Taylor Farms Maryland is recalling Wegmans Asian Chop Salad Kit, distributed in New York, Pennsylvania. The recall was initiated on 16 Jan 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesProduction batch number: WO2023013 Use by date: 01/26/2023
Quantity recalled810 bags

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-0349-2023
FDA event ID
91524
Recalling firm
Taylor Farms Maryland, Annapolis Junction, MD
Classification
Class I
Status
Terminated
Recall initiated
16 Jan 2023
FDA classified
10 Feb 2023
Reported
22 Feb 2023
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Milk
Product category
Salad Kits

Timeline

16 Jan 2023Recall initiated by company
10 Feb 2023Classified by FDA+25 days
22 Feb 2023Published in enforcement report+12 days

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

Reason for recall

Undeclared eggs and milk in salad

Product as listed by the FDA

Wegmans Asian Chop Salad Kit Net Wt. 13 OZ (368 g) Bag code date: TFMD013A5B. UPC: 077890512838.

Where it was distributed

Distributed to distribution centers in PA and NY.

New YorkPennsylvania

Stores named: Wegmans

Questions about this recall

Why was it recalled?

Undeclared eggs and milk in salad

Which lots are affected?

Production batch number: WO2023013 Use by date: 01/26/2023

Where was it sold?

Distributed to distribution centers in PA and NY.

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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