Knickerbocker 365 Inc.
FDA Regulatory Profile
Knickerbocker 365 Inc. has 1 FDA recall (1 Class I), 4 inspections, 0 510(k) clearances and 2 compliance actions on record.
- Latest recall
- F-1601-2023 · Class I · Sep 12, 2023
- Latest inspection
- Jun 6, 2025 · OAI
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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 | 4 | Nov 8, 2026 | Newest record Oct 28, 2026 | Current |
|---|
| Compliance actions | 2 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Recent Recalls
| Number | Class | Product | Date |
|---|
| F-1601-2023 | Class I | Knickerbocker Homestyle hamburger buns, 16oz, 8 count in clear plastic bag, UPC 6 11625 10020 6 | Sep 12, 2023 |
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 3003613292 | Madison Heights, MI | 4 | Jun 6, 2025 |