HUMAN MED AG
HUMAN MED AG appears in FDA public data with 1 recall, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1251-2025, Class II) was initiated on October 18, 2024. Its most recent 510(k) clearance was granted on June 29, 2010.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-1251-2025 | Class II | human med Biofill Infiltration Cannula, diameter 2.5mm, 15cm, REF 2024-012, REF 1580107, sterile, si | October 18, 2024 |