Leventon S. A. U.
Leventon S. A. U. appears in FDA public data with 1 recall, 0 510(k) clearances, 3 FDA inspections, and 1 compliance action on record. Its most recent recall (Z-2360-2019, Class II) was initiated on May 23, 2019.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 0
- Inspections
- 3
- Compliance Actions
- 1
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-2360-2019 | Class II | DOSI-FUSER 12591 5-500D1 -USA, 12591 5-600D1 -USA Provide parenteral drug infusions at a constant | May 23, 2019 |