Drug recall
Patient Side Cart Battery Box used in conjunction with the da Vinci A surgical system. Intuitive Surgical Inc…
FDA recall event 68593 · Class II · Intuitive Surgical, Inc.
Key facts
| Event ID | 68593 |
|---|---|
| Recall numbers | Z-1994-2014 |
| Recalling firm | Intuitive Surgical, Inc. |
| Product type | Devices |
| Products | Patient Side Cart Battery Box used in conjunction with the da Vinci A surgical system. Intuitive Surgical Inc. Sunnyvale, CA 94086 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Patient Side Cart battery boxes may overheat in rare charging conditions, causing battery bulging. |
| Initiation date | Apr 27, 2012 |
| Report date | Jul 16, 2014 |
| Termination date | Jul 7, 2014 |
| City | Sunnyvale |
| State | CA |
| Country | United States |
| FEI number | 3001675293 |
At a glance
- 1–9 Products in this recall
- 10–99 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: