Tuna, raw sold at meat counter and wrapped in butcher paper at point of purchase.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0353-2022.
Tuna tested above 50 ppm histamine.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0353-2022.
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 Sant' Elia Operations, 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-0353-2022.
Sant' Elia Operations, 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.
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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.
Sant' Elia Operations, Llc Recall FAQ
Sant' Elia Operations, Llc is the subject of a meat & poultry safety report: Tuna, raw sold at meat counter and wrapped in butcher paper at point of purchase.. The notice was published on October 26, 2021 by the U.S. Food and Drug Administration (FDA). Approximately 8 units are potentially affected.