CLASS I Food recall · Reported 4 Apr 2018 · FDA Enforcement Report

Cole Slaw, Store Made recalled by Weis Markets

Weis Markets is recalling Cole Slaw, Store Made, distributed in New York. The recall was initiated on 21 Mar 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesSell By: Mar 21, 2018 thru Mar 24, 2018
Quantity recalled~560 containers

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-0997-2018
FDA event ID
79599
Recalling firm
Weis Markets, Sunbury, PA
Classification
Class I
Status
Terminated
Recall initiated
21 Mar 2018
FDA classified
4 Apr 2018
Reported
4 Apr 2018
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Egg
Product category
Salad Kits

Timeline

21 Mar 2018Recall initiated by company
4 Apr 2018Classified by FDA+14 days
4 Apr 2018Published in enforcement report+0 days

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

Reason for recall

The ingredient label failed to declare egg because the store-made coleslaw scale label did not list the sub-ingredients of mayonnaise.

Product as listed by the FDA

Cole Slaw, Store Made. Packed in deli-style plastic containers: Weis, Weis Markets, Inc., Sunbury, PA; Cabbage, Carrots, Pineapple, White Onions, Sugar, Salt Pepper, Vinegar, Hellmanns Mayonnaise

Where it was distributed

NY

New York

Questions about this recall

Why was it recalled?

The ingredient label failed to declare egg because the store-made coleslaw scale label did not list the sub-ingredients of mayonnaise.

Which lots are affected?

Sell By: Mar 21, 2018 thru Mar 24, 2018

Where was it sold?

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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