FDA recall record

Da Vinci 5 ASSY,DV5 CONSOLE,IS5000 Foot Tray Pedals recall — FDA Z-1325-2025

Due to an increase in complaints concerning foot tray pedal spring failing resulting in the pedal remaining pressed

Class IIclassification
Z-1325-2025official record ID
Mar 19, 2025report date

Recall record at a glance

Official recordZ-1325-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmIntuitive Surgical, Inc.
Report dateMar 19, 2025
Recall initiation dateFeb 26, 2025
Quantity439 units
LocationSunnyvale, CA, United States

Official product description

Brand Name: Da Vinci 5 Product Name: ASSY,DV5 CONSOLE,IS5000 Foot Tray Pedals Model/Catalog Number: 380730 Software Version: N/A . Refer to HHE for additional details. Component: N/A

Why the product was recalled

Due to an increase in complaints concerning foot tray pedal spring failing resulting in the pedal remaining pressed

Distribution information

Worldwide distribution - US Nationwide and the countries of Alaska, Arizona, Arkansas, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin, Wyoming and the country of South Korea.

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.

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Class IIFDA: OngoingIntuitive Surgical, Inc.