FDA Device recall Z-1427-2013
Cannula 8MM Regular
- FDA Device
- Class II
- terminated
- Published 2013-06-05
On 2013-06-05 the FDA classified a Class II recall of Cannula 8MM Regular by Intuitive Surgical, citing clarification of existing labeling information and operating procedures.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1427-2013 |
| 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
Cannula 8MM Regular. Provides the means of introduction and placement of an instrument or accessory into the human body.
Reason
Clarification of existing labeling information and operating procedures.
Identifiers
| code_info | Model number 420002-07 |
|---|
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-1427-2013%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.