FDA recall record

Intuitive Surgical Da Vinci 5 ASSY, DV5 CONSOLE, IS5000 recall — FDA Z-1428-2026

An error event following the release of a software version for the surgical system that can result in loss of user interface content on an external…

Class IIclassification
Z-1428-2026official record ID
Feb 25, 2026report date

Recall record at a glance

Official recordZ-1428-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmIntuitive Surgical, Inc.
Report dateFeb 25, 2026
Recall initiation dateNov 17, 2025
Quantity12
LocationSunnyvale, CA, United States

Official product description

Da Vinci 5 ASSY, DV5 CONSOLE, IS5000 Model/Catalog Number: 380730 Used for minimally invasive surgery.

Why the product was recalled

An error event following the release of a software version for the surgical system that can result in loss of user interface content on an external monitor or tower monitor.

Distribution information

US distribution: LA, MA, NY, PA, TX, and VA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.

Medical DeviceJun 10, 2026

Da Vinci 5 ASSY,DV5 TOWER,IS5000 recall — FDA Z-2310-2026

Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching from the…

Class IIFDA: OngoingIntuitive Surgical, Inc.