FDA Device recall Z-1871-2014
IS4000 da Vinci Xi - Endoscope accessory
- FDA Device
- Class II
- terminated
- Published 2014-07-02
On 2014-07-02 the FDA classified a Class II recall of IS4000 da Vinci Xi - Endoscope accessory by Intuitive Surgical, citing in some procedures when using the endoscope in conjunction with the IS4000 (da Vinci Xi) System, the surgical view has an orange-yellow tint which can make it hard to differentiat….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1871-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-06-11 |
| Published | 2014-07-02 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Intuitive Surgical |
| Distribution | FL, NY, TX |
Product
IS4000 da Vinci Xi - Endoscope accessory; 0 Degree, 8mm Endoscope. Intuitive Surgical Inc.
Reason
In some procedures when using the endoscope in conjunction with the IS4000 (da Vinci Xi) System, the surgical view has an orange-yellow tint which can make it hard to differentiate between tissue
Identifiers
| code_info | 470026-18 |
|---|
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-1871-2014%22
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