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Terminated

Patient Side Cart Battery Box used in conjunction with the da Vinci A surgical system. Intuitive Surgical Inc. Sunnyvale, CA 94086

FDA Recall Z-1994-2014 · Posted 2014-07-04

Recalling FirmIntuitive Surgical, Inc.
Recall StatusTerminated
Product CodeNAY
Date Initiated2012-04-27
Date Terminated2014-07-07
Product Quantity2606

Reason for Recall

Patient Side Cart battery boxes may overheat in rare charging conditions, causing battery bulging.

Firm Action

No notification was sent. Issue is being addressed during routine maintenance or through complaint process.

Root Cause

Device Design

Distribution Pattern

Worldwide Distribution.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K081137INTUITIVE SURGICAL DA VINCI SI SURGICAL SYSTEM: MODEL IS3000Intuitive Surgical, Inc. · 2009-02-18K050369INTUITIVE SURGICAL DA VINCI SURGICAL SYSTEM, MODEL IS2000Intuitive Surgical, Inc. · 2005-04-29

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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