GRANDE PRODUCE LTD CO
FDA Regulatory Profile
GRANDE PRODUCE LTD CO has 1 FDA recall (1 Class I), 2 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest recall
- F-3467-2017 · Class I · Jul 21, 2017
- Latest inspection
- Jul 11, 2025 · NAI
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Summary
Record counts and when each FDA source was last refreshed
| Records | Count | Last refreshed | Source as of | Status |
|---|
| Recalls | 1 (1 Class I) | Nov 4, 2026 (checked Nov 8, 2026, unchanged) | File dated Nov 3, 2026 | Current |
|---|
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
|---|
| Inspections | 2 | Nov 10, 2026 | Newest record Nov 5, 2026 | Current |
|---|
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Recent Recalls
| Number | Class | Product | Date |
|---|
| F-3467-2017 | Class I | Caribena yellow maradol papaya packed in 35 pound cases | Jul 21, 2017 |
Recent FDA Inspections
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
| Facility | Location | Inspections | Latest |
|---|
| FEI 3006238219 | San Juan, TX | 2 | Jul 11, 2025 |