EPIX THERAPEUTICS, INC
EPIX THERAPEUTICS, INC appears in FDA public data with 6 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1320-2021, Class II) was initiated on February 22, 2021.
Summary
- Total Recalls
- 6
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-1320-2021 | Class II | EPIX Therapeutics DiamondTemp Bidrectional Large Curve Ablation Catheter, 7.5 French Size(2.48 mm), | February 22, 2021 |
| Z-1318-2021 | Class II | EPIX Therapeutics DiamondTemp Unidirectional Large Curve Ablation Catheter, 7.5 French Size(2.48 m | February 22, 2021 |
| Z-1317-2021 | Class II | EPIX Therapeutics DiamondTemp Unidirectional Small Curve Ablation Catheter, 7.5 French Size(2.48 mm | February 22, 2021 |
| Z-1322-2021 | Class II | EPIX Therapeutics DiamondTemp Unidirectional Ablation Catheter, Large Curve, 7.5 French Size(2.48 m | February 22, 2021 |
| Z-1319-2021 | Class II | EPIX Therapeutics DiamondTemp Bidrectional Small Curve Ablation Catheter, 7.5 French Size(2.48 mm), | February 22, 2021 |
| Z-1321-2021 | Class II | EPIX Therapeutics DiamondTemp Unidirectional Ablation Catheter, Small Curve, 7.5 French Size(2.48 | February 22, 2021 |