FDA Device recall Z-1994-2014
Patient Side Cart Battery Box used in conjunction with the da Vinci A surgical system
- FDA Device
- Class II
- terminated
- Published 2014-07-16
On 2014-07-16 the FDA classified a Class II recall of Patient Side Cart Battery Box used in conjunction with the da Vinci A surgical system by Intuitive Surgical, citing patient Side Cart battery boxes may overheat in rare charging conditions, causing battery bulging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1994-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-04-27 |
| Published | 2014-07-16 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Intuitive Surgical |
| Distribution | n/a |
Product
Patient Side Cart Battery Box used in conjunction with the da Vinci A surgical system. Intuitive Surgical Inc. Sunnyvale, CA 94086
Reason
Patient Side Cart battery boxes may overheat in rare charging conditions, causing battery bulging.
Identifiers
| code_info | Material number 371268-02 - al lots. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1994-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.