CLASS II Food recall · Reported 1 Oct 2014 · FDA Enforcement Report

Supreme Choice Jumbo Lump recalled by Supreme Distributors

Supreme Distributors is recalling Supreme Choice Jumbo Lump, distributed in Nevada. The recall was initiated on 30 Aug 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesALL
Quantity recalledN/A

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-2510-2014
FDA event ID
69150
Recalling firm
Supreme Distributors, Las Vegas, NV
Classification
Class II
Status
Terminated
Recall initiated
30 Aug 2014
FDA classified
22 Sep 2014
Reported
1 Oct 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Botulism
Product category
Crab & Lobster

Timeline

30 Aug 2014Recall initiated by company
22 Sep 2014Classified by FDA+23 days
1 Oct 2014Published in enforcement report+9 days

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

Reason for recall

Potential hazard of Clostridium botulinum toxin formation as a result of temperature abuse during storage.

Product as listed by the FDA

Supreme Choice brand Jumbo Lump, 16 oz; Premium Pasteurized Crab Meat. Product of Thailand. Distributed by Supreme Lobster and Seafood Company, Villa Park, IL 60181

Where it was distributed

NV only

Nevada

Questions about this recall

Is Supreme Choice Jumbo Lump recalled?

Yes. Supreme Distributors recalled Supreme Choice Jumbo Lump on 30 Aug 2014. The recall is Class II and its status is Terminated. Recall number F-2510-2014.

Why was it recalled?

Potential hazard of Clostridium botulinum toxin formation as a result of temperature abuse during storage.

Which lots are affected?

ALL

Where was it sold?

NV only

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 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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