WillowWood Global Llc
FDA Regulatory Profile
WillowWood Global Llc has 1 FDA recall, 2 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest recall
- Z-1594-2021 · Class II · Apr 20, 2021
- Latest inspection
- Feb 4, 2025 · NAI
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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 | 2 | Nov 8, 2026 | Newest record Oct 28, 2026 | Current |
|---|
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-1594-2021 | Class II | Alpha Interlock Suspension System Lanyard Body: An external prosthetic device. The Alpha Lanyard… | Apr 20, 2021 |
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 1522166 | Mount Sterling, OH | 2 | Feb 4, 2025 |