Epix Therapeutics recalls
Epix Therapeutics has 6 recalls on record with the FDA and USDA, the earliest in 2021 and the latest reported on 7 Apr 2021. 6 are still ongoing. The most frequent reason is sterility.
Total recalls6since 2021
Last 12 months0reported
Class I00% of total
Ongoing6latest 7 Apr 2021
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 6 100%Class III 0 0%
Why epix therapeutics is recalled
Product types
By year
Ongoing epix therapeutics recalls
6 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | DiamondTemp Unidirectional Large Curve Ablation Catheter recalled | Epix Therapeutics | Sterility | CA |
| Device | CLASS II | DiamondTemp Unidirectional Small Curve Ablation Catheter recalled | Epix Therapeutics | Sterility | CA |
| Device | CLASS II | DiamondTemp Bidrectional Small Curve Ablation Catheter Size recalled | Epix Therapeutics | Sterility | CA |
| Device | CLASS II | DiamondTemp Unidirectional Ablation Catheter recalled | Epix Therapeutics | Sterility | CA |
| Device | CLASS II | DiamondTemp Unidirectional Ablation Catheter recalled | Epix Therapeutics | Sterility | CA |
| Device | CLASS II | DiamondTemp Bidrectional Large Curve Ablation Catheter Size recalled | Epix Therapeutics | Sterility | CA |
All epix therapeutics recalls, newest first
6 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | DiamondTemp Unidirectional Large Curve Ablation Catheter recalled | Epix Therapeutics | Sterility | CA |
| Device | CLASS II | DiamondTemp Unidirectional Small Curve Ablation Catheter recalled | Epix Therapeutics | Sterility | CA |
| Device | CLASS II | DiamondTemp Bidrectional Small Curve Ablation Catheter Size recalled | Epix Therapeutics | Sterility | CA |
| Device | CLASS II | DiamondTemp Unidirectional Ablation Catheter recalled | Epix Therapeutics | Sterility | CA |
| Device | CLASS II | DiamondTemp Unidirectional Ablation Catheter recalled | Epix Therapeutics | Sterility | CA |
| Device | CLASS II | DiamondTemp Bidrectional Large Curve Ablation Catheter Size recalled | Epix Therapeutics | Sterility | CA |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.