Maradol Papaya; Frutas Selectas De Tijuana, S. DE R.L. DE, C.V. Sold in 14.00 kg/ 31 Lb. cardboard boxes.
⚠ 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-3560-2017.
Firm is recalling Maradol Papaya from Productores y Exportadores de Carica Papaya de Tecom¿n y Costa Alegre SPR of RL and packed by Frutas Selectas de Tijuana, S. de RL de CV due to Salmonella contamination
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-3560-2017.
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 Bravo 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-3560-2017.
Bravo 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.
Bravo Produce Inc Recall FAQ
Bravo Produce Inc is the subject of a food safety report: Maradol Papaya; Frutas Selectas De Tijuana, S. DE R.L. DE, C.V. Sold in 14.00 kg/ 31 Lb. cardboard boxes.. The notice was published on September 8, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 8,325 units are potentially affected.