Primus Corporation
Primus Corporation appears in FDA public data with 1 recall, 0 510(k) clearances, 7 FDA inspections, and 1 compliance action on record. Its most recent recall (Z-0321-2021, Class II) was initiated on October 9, 2020.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 0
- Inspections
- 7
- Compliance Actions
- 1
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-0321-2021 | Class II | Ultra2 Resolution Variants System for Abnormal Hemoglobin Quantitation | October 9, 2020 |