Caramel Apple packaged topped with colored sprinkles packaged in the following configurations with Best By Date range - 8/25-11/23/2014, ...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (listeria). 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-1218-2015.
CDC epidemiologists have linked an outbreak of Listeria monocytogenes illness to caramel apples.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1218-2015.
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 Lochirco Fruit & Produce 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-1218-2015.
Lochirco Fruit & Produce 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.
Lochirco Fruit & Produce Inc Recall FAQ
Lochirco Fruit & Produce Inc is the subject of a food safety report: Caramel Apple packaged topped with colored sprinkles packaged in the following configurations with Best By Date range - 8/25-11/23/2014, .... The notice was published on December 19, 2014 by the U.S. Food and Drug Administration (FDA). Approximately 123 units are potentially affected.