Drug recall
EVAC 70 XTRA with Integrated Cable REF EICA5872-01 Product Usage: PLASMA WAND devices are indicated for…
FDA recall event 71311 · Class II · ArthroCare Medical Corporation
Key facts
| Event ID | 71311 |
|---|---|
| Recall numbers | Z-1832-2015, Z-1833-2015 |
| Recalling firm | ArthroCare Medical Corporation |
| Product type | Devices |
| Products | EVAC 70 XTRA with Integrated Cable REF EICA5872-01 Product Usage: PLASMA WAND devices are indicated for ablation, resection, and coagulation of soft tissue and hemostasis of blood vessels in…, PROcise XP Wand with Integrated Cable REF EICA8872-01 Product Usage: PLASMA WAND devices are indicated for ablation, resection, and coagulation of soft tissue and hemostasis of blood vessels in… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Potential component failure causing device inoperability, Potential component failure resulting in inoperability |
| Initiation date | May 15, 2015 |
| Report date | Jul 1, 2015 |
| Termination date | Jun 27, 2016 |
| City | Austin |
| State | TX |
| Country | United States |
| FEI number | 3006524618 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: