FDA Device recall Z-1428-2013
Flush Port (used in almost all da Vinci instruments) Assists in cleaning the instrument
- FDA Device
- Class II
- terminated
- Published 2013-06-05
On 2013-06-05 the FDA classified a Class II recall of Flush Port (used in almost all da Vinci instruments) Assists in cleaning the instrument by Intuitive Surgical, citing clarification of existing labeling information and operating procedures.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1428-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2011-09-19 |
| Published | 2013-06-05 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Intuitive Surgical |
| Distribution | US |
Product
Flush Port (used in almost all da Vinci instruments) Assists in cleaning the instrument.
Reason
Clarification of existing labeling information and operating procedures.
Identifiers
| code_info | Model numbers: 340066-07 - straight; 340234-02 - extended taper; 340241-03 - 5mm; 340584-01 - Gemini 8mm straight;…Model numbers: 340066-07 - straight; 340234-02 - extended taper; 340241-03 - 5mm; 340584-01 - Gemini 8mm straight; 340586-02 - Gemini 5mm; 340725-01 - Vespa straight; 340800-01 - Gemini ext taper; 340971-01 - IS1200 Grasping 340972-01 IS2000 Grasping. |
|---|
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-1428-2013%22
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