Grove Grow Notes Fruit of Wolfberry (Fructus Lycii) Net Wt: 12 oz (340g) S & M (USA) Enterprise 4703 2nd Avenue Brooklyn, NY 11232 UPC 4...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (undeclared allergen). 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-0830-2014.
NYSDAM Sampling results has revealed the presence of undeclared sulfites in Fruit of Wolfberry.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0830-2014.
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 S & M International Inc 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-0830-2014.
S & M International Inc
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.
S & M International Inc Recall FAQ
S & M International Inc is the subject of a produce safety report: Grove Grow Notes Fruit of Wolfberry (Fructus Lycii) Net Wt: 12 oz (340g) S & M (USA) Enterprise 4703 2nd Avenue Brooklyn, NY 11232 UPC 4.... The notice was published on November 4, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 100 units are potentially affected.