Rovira Biscuit Corporation

FDA Regulatory Profile

Rovira Biscuit Corporation has 6 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest recall
H-0361-2026 · Class II · Dec 17, 2025
Latest inspection
Dec 17, 2025 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls6Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections7Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
H-0361-2026Class IIVanilla Treats Crackers, Rovira, Net Wt. 31 oz (878.83 g) cans, 6/31oz cans per case. Mini Vanilla…Dec 17, 2025
H-0360-2026Class IIVanilla Econo, Galletas de Vainilla, 8 paquets per Net Wt. 9.6 oz box (272 g), 6 box per case. UPC…Dec 17, 2025
H-0363-2026Class IITita Crackers Rovira, 3 (1/2 oz (15g) Foil Fresh Packets Net Wt.8 oz (226.8 g) boxes, 6/8oz boxes…Dec 17, 2025
H-0359-2026Class IITempting Crackers Tray, Rovira, 3 foil wrap trays per Net Wt. 8oz box (Net Wt 5 oz trays), 6 box per…Dec 17, 2025
H-0362-2026Class IIVainilla Crackers, Great Value (Galletas Vainilla)8 Foil Packets (17 g each), Net Wt.9.6 oz (272 g)…Dec 17, 2025
H-0358-2026Class IISnack Crackers 100to en boca (ciento en boca) Rovira, Net Wt. 1.5 oz, 12 pack Snack Crackers to go…Dec 17, 2025

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 17, 2025Ponce, PRFood/CosmeticsNo Action Indicated (NAI)2610242
Jun 14, 2023Ponce, PRFood/CosmeticsNo Action Indicated (NAI)2610242
Nov 26, 2019Ponce, PRFood/CosmeticsVoluntary Action Indicated (VAI)2610242
Oct 6, 2016Ponce, PRFood/CosmeticsNo Action Indicated (NAI)2610242
Mar 26, 2014Ponce, PRFood/CosmeticsVoluntary Action Indicated (VAI)2610242
Mar 31, 2011Ponce, PRFood/CosmeticsNo Action Indicated (NAI)2610242
Feb 18, 2009Ponce, PRFood/CosmeticsNo Action Indicated (NAI)2610242

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 2610242Ponce, PR7Dec 17, 2025

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.