Pharmasol Corporation
FDA Regulatory Profile
Pharmasol Corporation has 1 FDA recall, 10 inspections, 0 510(k) clearances and 1 compliance action on record.
- Latest recall
- D-0574-2022 · Class II · Jan 11, 2022
- Latest inspection
- Jun 14, 2021 · 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 | 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 | 10 | 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-0574-2022 | Class II | Lung Cleaner (saline eucalyptus) inhaler, 37 oz cans, Manufactured For: The Lung Cleaner LLC… | Jan 11, 2022 |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|
| Jun 14, 2021 | Stoughton, MA | Veterinary | Official Action Indicated (OAI) | 3014685473 |
| Jun 14, 2021 | South Easton, MA | Veterinary | Official Action Indicated (OAI) | 1250001 |
| Sep 5, 2018 | Stoughton, MA | Drugs | Official Action Indicated (OAI) | 3014685473 |
| Aug 20, 2018 | South Easton, MA | Drugs | Official Action Indicated (OAI) | 1250001 |
| Aug 4, 2016 | South Easton, MA | Drugs | Voluntary Action Indicated (VAI) | 1250001 |
| Jul 16, 2015 | South Easton, MA | Drugs | Voluntary Action Indicated (VAI) | 1250001 |
| Oct 30, 2014 | South Easton, MA | Drugs | Voluntary Action Indicated (VAI) | 1250001 |
| Oct 30, 2013 | South Easton, MA | Drugs | Voluntary Action Indicated (VAI) | 1250001 |
| Sep 27, 2011 | South Easton, MA | Drugs | Voluntary Action Indicated (VAI) | 1250001 |
| Sep 3, 2009 | South Easton, MA | Drugs | No Action Indicated (NAI) | 1250001 |
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.