Vilvet Pharmaceuticals Inc.
FDA Regulatory Profile
Vilvet Pharmaceuticals Inc. has 2 FDA recalls, 1 inspection, 0 510(k) clearances and 1 compliance action on record.
- Latest recall
- D-1487-2020 · Class II · Jul 24, 2020
- Latest inspection
- Jun 27, 2018 · 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 | 2 | 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 | 1 | Nov 9, 2026 | Newest record Oct 28, 2026 | Current |
| Compliance actions | 1 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Recent Recalls
| Number | Class | Product | Date |
| D-1487-2020 | Class II | VILAMIT MB (118 mg methenamine, 36 mg phenyl salicylate, 40.8 mg sodium phosphate monobasic, 10.0 mg… | Jul 24, 2020 |
| D-1488-2020 | Class II | VILEVEV MB Urinary Antispetic (81.0 mg methenamine, 40.8 mg sodium phosphate monobasic and 10.8 mg… | Jul 24, 2020 |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
| Jun 27, 2018 | Chester Springs, PA | Drugs | Official Action Indicated (OAI) | 3013511339 |
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 3013511339 | Chester Springs, PA | 1 | Jun 27, 2018 |