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Recall Observatory FDA recall evidence

Device product

da Vinci SP Surgical systems with the following Model Name/ Model Number / UDI: ASSY,PSS,SP1098,P4/ 380601-44/ 00886874114605 ASSY,SSC,SP1098,P4/ 380940-44 / 00886874114735 ASSY,VSS,SP1098,P4/ 380941-44 / 00886874114742 SOFTWARE, SYSTEM EMBEDDED RLS, SP1098, B70_P4_B327 (OS4 v4.0.0 (P4_B327) / 610112-327 / N/A

Z-0419-2022

September 22, 2021

Class II

Product summary

Firm
Intuitive Surgical, Inc.
Event
Event 89109
Status
Ongoing
Classification
Class II
Quantity
46
Official record key
device-enforcement:Z-0419-2022

Official wording

Reason: Issue was identified during internal engineering evaluation. Use of the system with the affected software version may experience either an inability to deliver energy or an inadvertent delivery of energy. Use may require surgeon to resolve an injury or need moderate intraoperative intervention. Also, use may potentially cause user frustration or a minor delay to troubleshoot.

Code information: All da Vinci SP Surgical systems with software version OS4 v4.0.0 (P4_B327)

Distribution pattern: US Nationwide distribution in the states of Arizona, California, Connecticut, Florida, Illinois, Kansas, Kentucky, Massachusetts, Minnesota, Missouri, New Jersey, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Tennessee, Texas, Virginia, Washington, and Wisconsin.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software version may experience either an inability to deliver energy or an inadvertent delivery of energy. Use may