ProtiDiet High Protein Chocolate Dream Bar
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (Salmonella contamination). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1270-2013.
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.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1270-2013.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Doctors Best Weight Loss or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1270-2013.
Doctors Best Weight Loss
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Doctors Best Weight Loss Recall FAQ
Doctors Best Weight Loss is the subject of a snacks & candy safety report: ProtiDiet High Protein Chocolate Dream Bar. The notice was published on March 8, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 3 units are potentially affected.