CLASS II Food recall · Reported 5 Feb 2020 · FDA Enforcement Report

Krab Salad recalled by ASK Foods

ASK Foods is recalling Krab Salad, distributed in Maryland. The recall was initiated on 7 Jan 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesProduct Number 2786-140 Date code of 2242 Sell by date of 1/18/2020
Quantity recalled154 - 5 lb. bulk 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-0565-2020
FDA event ID
84699
Recalling firm
ASK Foods, Palmyra, PA
Brand
Krab
Classification
Class II
Status
Terminated
Recall initiated
7 Jan 2020
FDA classified
28 Jan 2020
Reported
5 Feb 2020
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Foreign Material
Product category
Salad Kits

Timeline

7 Jan 2020Recall initiated by company
28 Jan 2020Classified by FDA+21 days
5 Feb 2020Published in enforcement report+8 days

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

Reason for recall

The product has the potential to contain metal pieces.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

ASK Foods Inc., KRAB SALAD, NET WT. 5 LB (2.27 kg), Plastic tub with a plastic lid,Keep Refrigerated, 2786-140

Where it was distributed

MD

Maryland

Questions about this recall

Why was it recalled?

The product has the potential to contain metal pieces.

Which lots are affected?

Product Number 2786-140 Date code of 2242 Sell by date of 1/18/2020

Where was it sold?

MD

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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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