RecallRadar

FDA Device recall Z-1687-2013

da Vinci Si Vision System Cart, model number VS3000

On 2013-07-17 the FDA classified a Class II recall of da Vinci Si Vision System Cart, model number VS3000 by Intuitive Surgical, citing factory testing on da Vinci Si Surgical Systems may not be in compliance with UL Standards as one of the testing devices was found to be working incorrectly.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1687-2013
ClassificationClass II
Statusterminated
Initiated2013-06-08
Published2013-07-17
Last updated2026-09-13 11:53 UTC
CompanyIntuitive Surgical
DistributionAZ, CA, CO, FL, HI, MT, NY, TX, UT, WA

Product

da Vinci Si Vision System Cart, model number VS3000; Manufactured by Intuitive Surgical, Sunnyvale, CA 94086. Intuitive Surgical endoscopic Instrument Control System is intended to assist in the accurate control of Intuitive Surgical Endoscopic instruments. It is intended for adult and pediatric use.

Reason

Factory testing on da Vinci Si Surgical Systems may not be in compliance with UL Standards as one of the testing devices was found to be working incorrectly.

Identifiers

code_info
Part number 380990-11: Serial numbers: 324350 325289 325301 325858 325872 325686 325700 325639 325646 32453…Part number 380990-11: Serial numbers: 324350 325289 325301 325858 325872 325686 325700 325639 325646 324537 324566 324087 324577 324772 324784 324948 325126 325279 325138 325621 325441 325453 325564 323865 323870 323977 324010 324014 324334.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1687-2013%22

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