Data Foundry

Medical device recalls 2022

Da Vinci S/Si Large Clip Applier — Class II medical device recall Z-1459-2022

Ongoing recall by Intuitive Surgical, Inc., reported 2022-08-03, distributed nationwide. Due to the potential for unexpected motion caused by the partial disengagement of the instrument from the syst

Recall numberZ-1459-2022
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmIntuitive Surgical, Inc., Sunnyvale, CA, United States
Recall initiated2022-07-01
Classified2022-07-25
Reported by FDA2022-08-03
DistributedNationwide (US)
Countries outside the USAE, AR, AT, AU, BE, BG, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DK, DO, EC, ES, FI, FR, GB, GR, HK, HU, ID, IE, IL, IN, IS, IT, JP, KR, KW, KY, LB, LU, MT, MX, MY, NL, NO, NZ, PA, PH, PK, PL, PT, QA, RO, SA, SE, SG, SI, SK, TH, TR, TW, UY, VE, VN, ZA
Quantity62,895 clip
UPC / GTIN / UDI-DI00886874111161, 00886874111680, 00886874111826
Model numbers420003, 420230, 420327

Product

Da Vinci S/Si Large Clip Applier, Model 420230 Da Vinci S/Si Medium-Large Clip Applier, Model 420327 Da Vinci S/Si Small Clip Applier, Model 420003

Reason for recall

Due to the potential for unexpected motion caused by the partial disengagement of the instrument from the system.

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-1459-2022. 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.