Cannula 8MM Regular — Class II medical device recall Z-1427-2013
Terminated recall by Intuitive Surgical, Inc., reported 2013-06-05, distributed nationwide. Clarification of existing labeling information and operating procedures.
| Recall number | Z-1427-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Intuitive Surgical, Inc., Sunnyvale, CA, United States |
| Recall initiated | 2011-09-19 |
| Classified | 2013-05-29 |
| Reported by FDA | 2013-06-05 |
| Terminated | 2013-05-30 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, AU, CA, CL, CN, CZ, EG, ES, IL, IN, IT, KR, PL, QA, RO, SA, SG, TH, TR, VE |
| Reason classes | labeling |
| Model numbers | 420002-07 |
Product
Cannula 8MM Regular. Provides the means of introduction and placement of an instrument or accessory into the human body.
Reason for recall
Clarification of existing labeling information and operating procedures.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1427-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.