CB1102052 BOCATA ESPECIAL CASERO'S
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1278-2022.
Finished product potentially adulterated with insect filth.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1278-2022.
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 Gruvipa S.l. 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-1278-2022.
GRUVIPA S.L.
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.
Gruvipa S.l. Recall FAQ
Gruvipa S.l. is the subject of a food safety report: CB1102052 BOCATA ESPECIAL CASERO'S. The notice was published on May 23, 2022 by the U.S. Food and Drug Administration (FDA). Approximately 116,160 units are potentially affected.