Dark Chocolate Dolcini, In clear plastic cup, 72 individual servings, Store frozen
⚠ 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-1230-2017.
Dark Chocolate Dolcini and Limoncello Dolcini were made using ingredients which was allegedly affected by the dry milk recall from Valley Milk and could potentially be contaminated with Salmonella.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1230-2017.
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 Steven Roberts Originals, Llc 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-1230-2017.
Steven Roberts Originals, LLC
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.
Steven Roberts Originals, Llc Recall FAQ
Steven Roberts Originals, Llc is the subject of a snacks & candy safety report: Dark Chocolate Dolcini, In clear plastic cup, 72 individual servings, Store frozen. The notice was published on December 9, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 372 units are potentially affected.