Data Foundry

Medical device recalls 2020

Da Vinci Xi/X EndoWrist Monopolar Curved scissors — Class II medical device recall Z-1105-2020

Terminated recall by Intuitive Surgical, Inc., reported 2020-02-12, distributed in AL, AZ, CA, CO, CT, DE, FL, GA…. This recall is being initiated because lots of EndoWrist Monopolar Curved Scissor instruments are not recogniz

Recall numberZ-1105-2020
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmIntuitive Surgical, Inc., Sunnyvale, CA, United States
Recall initiated2018-12-04
Classified2020-02-06
Reported by FDA2020-02-12
Terminated2022-08-24
DistributedAL, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KY, LA, MA, MD, MI, MN, MO, MT, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, TN, TX, VA, VT, WA, WI, WV, WY
Quantity286 monopolar
UPC / GTIN / UDI-DI00886874112298
Lot numbersN11181003, N11181004
Model numbers470179-19

Product

Da Vinci Xi/X EndoWrist Monopolar Curved scissors (MCS), model number 470179-19, UDI: (00) 886874112298

Reason for recall

This recall is being initiated because lots of EndoWrist Monopolar Curved Scissor instruments are not recognized by the integrated electrosurgical unit, which prohibits the activation of monopolar energy from the surgeon console.

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-1105-2020. 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.