Degasa Sa De Cv
Degasa Sa De Cv has 1 FDA recall, 0 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest recall
- D-1129-2017 · Class II · Aug 4, 2017
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Summary
| 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 | 0 | Nov 9, 2026 | Newest record Oct 28, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Related names
| Name | Recalls | 510(k) | Inspections | Compliance | Most recent recall |
|---|---|---|---|---|---|
| Degasa S.A. De C.V | 0 | 0 | 2 | 1 | — |
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| D-1129-2017 | Class II | Povidone Iodine, USP Prep Solution, 10%, packaged in 1 gallon bottle, OTC, Manufactured for PSS… | Aug 4, 2017 |