Palmer's Candies Creme De Menthe Bark, A) NET WT 9 OZ (255 g) packaged in cardboard boxes, UPC Code 77232-16043, B) NET WT 9 OZ (255 g) p...
⚠ 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-1498-2017.
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1498-2017.
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 Palmer And Company, Dba Palmer Candy Co 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-1498-2017.
Palmer and Company, dba Palmer Candy Co
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.
Palmer And Company, Dba Palmer Candy Co Recall FAQ
Palmer And Company, Dba Palmer Candy Co is the subject of a food safety report: Palmer's Candies Creme De Menthe Bark, A) NET WT 9 OZ (255 g) packaged in cardboard boxes, UPC Code 77232-16043, B) NET WT 9 OZ (255 g) p.... The notice was published on January 9, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 1 units are potentially affected.