Intuitive Surgical Inc — Class II medical device recall Z-2020-2014
Terminated recall by Intuitive Surgical, Inc., reported 2014-07-16. Manufacturing variation in the grip assembly of the Large Clip applier which can lead to the instrument jammin
| Recall number | Z-2020-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Intuitive Surgical, Inc., Sunnyvale, CA, United States |
| Recall initiated | 2014-06-13 |
| Classified | 2014-07-08 |
| Reported by FDA | 2014-07-16 |
| Terminated | 2014-12-01 |
| Lot numbers | M10120516, M10120523, M10120529, M10120530, M10120607, M10120615, M10120627, M10120628, M10120629, M10120702, M10120704, M10120706, M10120712, M10120716, M10120718, M10120724, M10120727, M10120731, M10120803, M10120807, M10120813, M10120817, M10120827, M10120830, M10120911, M10120918, M10120925, M10121001, M10121009, M10121015, M10121025, M10121030, M10121105, M10121113, M10121116, M10121126, M10121128, M10121203, M10121205, M10121207 and 79 more |
| Model numbers | 420230-04, 420230-06 |
Product
Intuitive Surgical Inc. Large Clip Applier instruments used in conjunction with da Vinci S and da Vinci SI Surgical Systems Intuitive Surgical Inc., 'Sunnyvale, CA 94086
Reason for recall
Manufacturing variation in the grip assembly of the Large Clip applier which can lead to the instrument jamming during insertion when used with the 8 mm cannula or with certain reducer accessories..
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-2020-2014. 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.