CLASS I Food recall · Reported 3 Apr 2013 · FDA Enforcement Report

ProtiDiet High Protein Chocolate Dream Bar recalled

Doctors Best Weight Loss is recalling ProtiDiet High Protein Chocolate Dream Bar. The recall was initiated on 8 Mar 2013 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUPC 6 21498 42238 1, lot code CR 18 13B, and Best Before: 2015-08.
Quantity recalled3 boxes (21 bars in total)

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-1270-2013
FDA event ID
64606
Recalling firm
Doctors Best Weight Loss, Pembroke Pines, FL
Classification
Class I
Status
Terminated
Recall initiated
8 Mar 2013
FDA classified
26 Mar 2013
Reported
3 Apr 2013
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Salmonella
Product category
Chocolate

Timeline

8 Mar 2013Recall initiated by company
26 Mar 2013Classified by FDA+18 days
3 Apr 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

Recall was initiated after CFIA notified FDA of implicated products sold to the firm. During a FDA visit, the firm discovered that they were selling product that were recalled in Canada by the manufacturer, "Pro-Amino International Inc." because it may be contaminated with Salmonella. Upon further FDA investigation at the firm product was further distributed to a consignee in Canada.

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

ProtiDiet High Protein Chocolate Dream Bar

Where it was distributed

Canada

Questions about this recall

Why was it recalled?

Recall was initiated after CFIA notified FDA of implicated products sold to the firm. During a FDA visit, the firm discovered that they were selling product that were recalled in Canada by the manufacturer, "Pro-Amino International Inc." because it may be contaminated with Salmonella. Upon further FDA investigation at the firm product was further distributed to a consignee in Canada.

Which lots are affected?

UPC 6 21498 42238 1, lot code CR 18 13B, and Best Before: 2015-08.

Where was it sold?

Canada

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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