CLASS I Food recall · Reported 20 Feb 2013 · FDA Enforcement Report

Cucumbers/box recalled by Altiza

Altiza is recalling Cucumbers/box, distributed in California. The recall was initiated on 28 Jan 2013 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot #MA012304.
Quantity recalled343 units

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-0984-2013
FDA event ID
35782
Recalling firm
Altiza, Chula Vista, CA
Classification
Class I
Status
Terminated
Recall initiated
28 Jan 2013
FDA classified
12 Feb 2013
Reported
20 Feb 2013
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Salmonella
Product category
Cucumbers

Timeline

28 Jan 2013Recall initiated by company
12 Feb 2013Classified by FDA+15 days
20 Feb 2013Published 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

Altiza is recalling Malichita brand cucumbers because they may be contaminated with Salmonella.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Cucumbers, 44 lbs/box. Brand: Malichita (green, yellow, red and white background color on each cartons)

Where it was distributed

CA

California

Questions about this recall

Is Cucumbers/box recalled?

Yes. Altiza recalled Cucumbers/box on 28 Jan 2013. The recall is Class I and its status is Terminated. Recall number F-0984-2013.

Why was it recalled?

Altiza is recalling Malichita brand cucumbers because they may be contaminated with Salmonella.

Which lots are affected?

Lot #MA012304.

Where was it sold?

CA

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 21 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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