NDAL Mfg Inc.
NDAL Mfg Inc. has 1 FDA recall (1 Class I), 0 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest recall
- D-0269-2021 · Class I · Dec 17, 2020
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 1 (1 Class I) | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 0 | Nov 13, 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 |
|---|---|---|---|
| D-0269-2021 | Class I | ManukaGuard Medical Grade Manuka Honey Allercleanse Nasal Spray, 1.3 FL OZ (40mL) bottle, 270… | Dec 17, 2020 |
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