Intuitive Surgical, Inc. recalls
Every recall we track for Intuitive Surgical, Inc. — 106 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Intuitive Surgical, Inc. fell by more than half in 2025 (13, down from 42 in 2024). 1% rated “stop using now”.
All FDA recall records for Intuitive Surgical, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 2 | 0 | 0 | 2 |
| 2018 | 1 | 8 | 4 | 0 | 13 |
| 2019 | 0 | 8 | 5 | 0 | 13 |
| 2020 | 0 | 2 | 1 | 0 | 3 |
| 2021 | 0 | 3 | 1 | 0 | 4 |
| 2022 | 0 | 7 | 1 | 0 | 8 |
| 2023 | 0 | 4 | 0 | 0 | 4 |
| 2024 | 0 | 42 | 0 | 0 | 42 |
| 2025 | 0 | 7 | 6 | 0 | 13 |
| 2026 (to date) | 0 | 3 | 1 | 0 | 4 |
What to do if you have a recalled Intuitive Surgical, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Intuitive Surgical, Inc. recalls
54 shown- Use cautionMedical device
Intuitive Surgical, Inc. recalls Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000 Model/Catalog Number: 380746 Software Version: N/A Product
Intuitive Surgical recalls Da Vinci 5 dV5 Tower NIR handheld camera (model 380746) due to unintentional activation during normal surgical workflow transitions, potentially causing unintended illumination. Affected units have specific serial numbers listed in the recall notice.
Intuitive SurgicalApr 24, 2026 - Use cautionMedical device
Intuitive Surgical, Inc. recalls Da Vinci ASSY, PSS, SP1098, Part Number: 380601
Intuitive Surgical recalls Da Vinci surgical systems with specific part numbers due to potential E-brake pin failure causing uncontrolled motion and patient injury.
Intuitive SurgicalApr 22, 2026 - Use cautionMedical device
Intuitive Surgical, Inc. recalls Brand Name: Da Vinci X and Da Vinci Xi Product Name: da Vinci X, Xi Surgical System Model/Catalog Number: IS4000;
Intuitive Surgical recalls Da Vinci X and Xi surgical systems with model IS4000/IS4200 due to potential broken screws in manipulator arms, which could cause injury during surgery.
Intuitive SurgicalApr 2, 2026 - Lower riskMedical device
Intuitive Surgical, Inc. recalls Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06
Intuitive Surgical recalls 8 mm SureForm 30 Gray Reloads (reference numbers 48230M-05 and 48230M-06) due to potential incomplete staple lines during use.
Intuitive SurgicalMar 11, 2026 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci 5 Surgeon Console Viewer Display, ASSY, DV5 CONSOLE, IS5000, Part Number: 380730-45
Intuitive Surgical recalls da Vinci 5 Surgeon Console Viewer Display units with outdated firmware that may cause loss of 3D surgical field, potentially leading to injury during robotic-assisted surgery.
Intuitive SurgicalDec 30, 2025 - Lower riskMedical device
Intuitive Surgical, Inc. recalls da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073 (2.7-4cm,SP1098, Box) & 430075
Intuitive Surgical recalls da Vinci SP Access Port Kits with reference numbers 430073 and 430075 due to potential cracks causing sterility breaches. Affected units include specific lot numbers and sizes.
Intuitive SurgicalDec 15, 2025 - Use cautionMedical device
Intuitive Surgical, Inc. recalls Brand Name: da Vinci S, Si Mega Needle Driver Instrument Product Name: da Vinci S, Si Mega Needle Driver Instrument
Intuitive Surgical recalls da Vinci S/Si Mega Needle Driver instruments with potential broken or frayed grip cables. These reusable surgical tools may cause injury if cables fail during use.
Intuitive SurgicalDec 9, 2025 - Use cautionMedical device
Intuitive Surgical, Inc. recalls Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument Product Name: da Vinci S, Si Permanent Cautery Hook
Intuitive Surgical recalls da Vinci S/Si reusable cautery hook instruments with frayed or broken pitch cables that could cause injury during surgery. Affected models include 420183.
Intuitive SurgicalDec 9, 2025 - Lower riskMedical device
Intuitive Surgical, Inc. recalls Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog Number: 490127 Software Version:
Intuitive Surgical recalls Ion Vision Probe Bags (model 490127) due to potential compromised sterile pouch seals. These single-use bags, used with their robotic surgery system, may not be sterile after packaging. Affected units include specific batch numbers listed in the recall notice.
Intuitive SurgicalDec 4, 2025 - Lower riskMedical device
Intuitive Surgical, Inc. recalls Da Vinci 5 ASSY, DV5 CONSOLE, IS5000 Model/Catalog Number: 380730 Used for minimally invasive surgery.
Intuitive Surgical recalls Da Vinci 5 surgical systems with model 380730 that may lose monitor content due to a software error. Affected units have specific UDI-DI and software version.
Intuitive SurgicalNov 17, 2025 - Use cautionMedical device
Intuitive Surgical, Inc. recalls Brand Name: Da Vinci Product Name: da Vinci X, Xi Surgical System, & da Vinci 5 Surgical System Model/Catalog Number:
Intuitive Surgical recalls Da Vinci X, Xi, and 5 surgical systems due to a software error that allows malfunctioning instrument arms to remain in use, potentially leading to ball screw fatigue failure.
Intuitive SurgicalNov 7, 2025 - Lower riskMedical device
Intuitive Surgical, Inc. recalls da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15
Intuitive Surgical recalls da Vinci SP Instrument Arm Drape, SP, 1-PACK (Part Numbers 430013-13, 430013-15) due to potential detachment of drapes causing procedure delays. Affected units sold with specific lot numbers.
Intuitive SurgicalMay 12, 2025 - Use cautionMedical device
Intuitive Surgical, Inc. recalls Brand Name: Da Vinci 5 Product Name: ASSY,DV5 CONSOLE,IS5000 Foot Tray Pedals Model/Catalog Number: 380730 Software
Intuitive Surgical recalls Da Vinci 5 foot tray pedals with model 380730 manufactured before December 20, 2024. Pedals may stay pressed causing discomfort or injury during surgery.
Intuitive SurgicalFeb 26, 2025 - Use cautionMedical device
Intuitive Surgical, Inc. recalls 8MM, Small Graptor REF 470318 Is a grasping retractor Instrument used with the da Vinci X/Xi Surgical Systems in a wide
Intuitive Surgical recalls 8MM Small Graptor REF 470318 instruments used with da Vinci X/Xi surgical systems due to reported pitch cable failures that could cause instrument malfunction during procedures.
Intuitive SurgicalDec 19, 2024 - Use cautionMedical device
Intuitive Surgical, Inc. recalls 8MM,HORIZON SMALL CLIP APPLIER,IS4000¿ REF 470401
Intuitive Surgical recalls Horizon Small Clip Applier models with frayed grip cables that could cause injury during surgery. Affected units include specific batch numbers and model 470401.
Intuitive SurgicalDec 19, 2024 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci 5, Surgeon Console Column Motor Connector; ASSY,DV5 CONSOLE,SSC,IS5000; Part Number: 380730-40
Intuitive Surgical recalls da Vinci 5 surgeon console column motor connectors with serial numbers listed. Partially damaged connectors cause ergonomics errors that may delay or abort surgery until replaced.
Intuitive SurgicalAug 21, 2024 - Use cautionMedical device
Intuitive Surgical, Inc. recalls Ion Endoluminal System, REF: 380748-65
Intuitive Surgical recalls Ion Endoluminal System (REF: 380748-65) due to potential screw failure causing uncontrolled catheter movement in airways. Affected units have specific serial numbers.
Intuitive SurgicalJul 12, 2024 - Use cautionMedical device
Intuitive Surgical, Inc. recalls Patient Cart, Part: 380601, a component of the da Vinci SP Surgical System, Model: SP1098
Intuitive Surgical recalls Patient Cart Part 380601 for da Vinci SP Surgical System Model SP1098. Inadequately welded belts may cause tissue injuries or pinching injuries to the user during surgery.
Intuitive SurgicalMar 13, 2024 - Use cautionMedical device
Intuitive Surgical, Inc. recalls Da Vinci Single-Site Wristed Needle Driver, REF: 478115, 5 mm
Intuitive Surgical recalls Da Vinci Single-Site Wristed Needle Driver REF 478115 (5mm) due to potential dislodgement or breakage causing uncontrolled movement. Affected units have specific serial numbers.
Intuitive SurgicalOct 6, 2023 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci Xi/X Tip-Up Fenestrated Grasper, REF: 470347, VER: 12
Intuitive Surgical recalls da Vinci Xi/X Tip-Up Fenestrated Graspers with potential for stainless steel fragments to fall into patients during surgery.
Intuitive SurgicalJun 12, 2023 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci Xi Surgical System Model IS4000 da Vinci X Surgical System Model IS4200
Intuitive Surgical recalls da Vinci Xi (IS4000) and X (IS4200) surgical systems with loose Universal Surgical Manipulator carriage due to manufacturing defects. Affected units have specific serial numbers.
Intuitive SurgicalFeb 10, 2023 - Use cautionMedical device
Intuitive Surgical, Inc. recalls Patient Side Cart, REF: 380620, with instrument arms, used as part of the da Vinci X Surgical System, REF: IS4200;
Intuitive Surgical recalls Patient Side Carts (REF: 380620/380652) used with da Vinci X/Xi systems due to potential instrument arm failure causing tissue injury. Affected units include specific serial numbers.
Intuitive SurgicalJan 24, 2023 - Use cautionMedical device
Intuitive Surgical, Inc. recalls INTUITIVE Da Vinci Xi 8mm SureForm 30 Curved-Tip Stapler Da Vinci Xi|X REF 488530 INTUITIVE Da Vinci 8mm SureForm 30
Intuitive Surgical recalls Da Vinci Xi 8mm SureForm 30 Curved-Tip Staplers due to potential staple deployment failure and device fragment generation. Affected models include specific colors and serial numbers.
Intuitive SurgicalOct 7, 2022 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci X (IS4200) and Xi (IS4000) systems, which consists of finished devices Surgeon Console (SSC), Patient Cart
Intuitive Surgical recalls da Vinci X and Xi surgical systems with software version P10 due to risk of unintended energy delivery causing injury if specific conditions are met.
Intuitive SurgicalSep 20, 2022 - Use cautionMedical device
Intuitive Surgical, Inc. recalls Da Vinci S/Si Large Clip Applier, Model 420230 Da Vinci S/Si Medium-Large Clip Applier, Model 420327 Da Vinci S/Si
Intuitive Surgical recalls Da Vinci S/Si Large, Medium-Large, and Small Clip Appliers due to potential unexpected motion from partial disengagement. Affected units include specific models and serial numbers.
Intuitive SurgicalJul 1, 2022 - Lower riskMedical device
Intuitive Surgical, Inc. recalls The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit (ESU) designed to be used with the da Vinci Xi and
Intuitive Surgical recalls E-100 Generators (PN 374848-09) due to preventative maintenance not being performed, which could lead to malfunction when used with da Vinci Xi and X systems.
Intuitive SurgicalJun 22, 2022 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinici X da Vinci Xi Sureform 45 REF 480445 da Vinci X da Vinci Xi Sureform 45 Curved-Tip REF 480545 da Vinici X da
Intuitive Surgical recalls da Vinci Xi Sureform 45 and Curved-Tip models due to tissue pushout events causing bleeding risks during surgery. Affected units include specific model numbers and serial codes.
Intuitive SurgicalMar 17, 2022 - Use cautionMedical device
Intuitive Surgical, Inc. recalls VESSEL SEALER EXTEND, Single-Use Instrument EndoWrist Instruments 8mm, da Vinci X' da Vinci Xi', REF 480422
Intuitive Surgical recalls da Vinci X/Xi vessel sealers with 8mm EndoWrist instruments (REF 480: 00886874115664) due to risk of insufficient seal when excessive tissue is placed in jaws.
Intuitive SurgicalMar 3, 2022 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci Xi and X 12-8 mm Conductive Cannula Reducer, REF: 470381-11
Intuitive Surgical recalls da Vinci Xi and X 12-8 mm Conductive Cannula Reducer (REF: 470381-11) due to risk of metal tip dislodging, potentially causing tissue damage or bowel obstruction if not removed during surgery.
Intuitive SurgicalDec 23, 2021 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci SP Surgical systems with the following Model Name/ Model Number / UDI: ASSY,PSS,SP1098,P4/ 380601-44/
Intuitive Surgical recalls da Vinci SP Surgical systems with specific software versions that may experience energy delivery problems, requiring surgeon intervention or causing delays. Affected units include models with UDI codes listed in the recall notice.
Intuitive SurgicalSep 22, 2021 - Lower riskMedical device
Intuitive Surgical, Inc. recalls The da Vinci Xi and X surgical systems (IS4000 and IS4200) each consist of three main components: the Surgeon Console
Intuitive Surgical recalls da Vinci Xi and X surgical systems (IS40:000 and IS4200) due to incorrect expiration dates on packaging, which could lead to improper use of sterile components.
Intuitive SurgicalSep 21, 2021 - Use cautionMedical device
Intuitive Surgical, Inc. recalls Ion Flexison Biopsy Needle, 19G, Extension Range : 0-3 cm, Ref: 490104-09 and 49004-10, 5-pack, Sterile EO, Rx only,
Intuitive Surgical recalls 5-packs of 19G Ion Flexison Biopsy Needles with potential sheath tip separation. Affected lots include S90200303 to S90210414. Contact for remedy.
Intuitive SurgicalAug 6, 2021 - Use cautionMedical device
Intuitive Surgical, Inc. recalls Box Label: ION Fully Articulating Catheter, REF 490105, VER 08 - Product Usage: used to navigate the Ion Fully
Intuitive Surgical recalls ION Fully Articulating Catheter model 490105-08 (VER 08) due to risk of distal tip ring dislodging during procedures. All units with serial numbers listed may be affected.
Intuitive SurgicalOct 23, 2020 - Lower riskMedical device
Intuitive Surgical, Inc. recalls Ion Catheter Reprocessing Cover, IF1000 (Part Number:490114-02) UDI:00886874116845.
Intuitive Surgical recalls Ion Catheter Reprocessing Cover model IF1000 (Part 490114-02) due to potential cleaning chemical retention during reprocessing, which may cause system failure.
Intuitive SurgicalJun 10, 2020 - Lower riskMedical device
Intuitive Surgical, Inc. recalls STAINLESS STEEL REPROCESSING TRAY, 8MM ENDOSCOPE, IS4000, Model No. 400498-02 - Product Usage: is designed to enable
Intuitive Surgical recalls stainless steel reprocessing trays for 8mm endoscopes due to potential sterility breaches from small holes in sterilization wraps. Affected units include Model 400498-02 with all batch numbers.
Intuitive SurgicalDec 19, 2019 - Lower riskMedical device
Intuitive Surgical, Inc. recalls da Vinci SP Camera; PN 430060-33; Model Number: 430060-33. For endoscopic surgery.
Intuitive Surgical recalls da Vinci SP Camera model 430060-33 due to residual soil on camera tips that could cause image issues or sensitization risks during surgery.
Intuitive SurgicalAug 19, 2019 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci X Surgical System Surgical System, IS4200, 00886874114216 Product Usage: used with an endoscope, surgical
Intuitive Surgical recalls da Vinci X surgical systems with defective capacitors that could cause vision loss or system errors. Affected units have specific serial numbers; contact for remedy.
Intuitive SurgicalJul 26, 2019 - Use cautionMedical device
Intuitive Surgical, Inc. recalls daVinci XI Sureform 60 Reload, 60 mm black 6-Row 4.6 mm, Ref: 48360T-08 , UDI: 00886874113851, Rx only, SterileEO -
Intuitive Surgical recalls daVinci XI Sureform 60 Reload staples that may not deploy staples properly, risking air leaks during surgery. Affected units have specific lot numbers and are used in certain surgical procedures.
Intuitive SurgicalJul 1, 2019 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci Surgical System, IS 4000; Endoscope Controller, Model Number: 372601-16 (UDI: 00886874114193) is included in
Intuitive Surgical recalls da Vinci Xi Endoscope Controller Model 372601-16 due to improper calibration causing potential thermal tissue injury and overly bright images during surgery.
Intuitive SurgicalJun 17, 2019 - Use cautionMedical device
Intuitive Surgical Inc recalls da Vinci X Surgical System, IS4200 - Product Usage: The da Vinci Xi surgical system (IS4000) is made of three main
Intuitive Surgical recalls da Vinci Xi surgical systems (IS4000) with high friction in universal surgical manipulators causing resistance, hesitation, and jerking during use. Affected units have specific serial numbers and UDI codes.
Intuitive SurgicalApr 11, 2019 - Lower riskMedical device
Intuitive Surgical, Inc. recalls da Vinci SP surgical system
Intuitive Surgical recalls da Vinci SP surgical systems with specific serial numbers due to rare vibration risk when using Adjust Mode near vertical position limit and sustained force on hand controls.
Intuitive SurgicalApr 1, 2019 - Lower riskMedical device
Intuitive Surgical, Inc. recalls daVinci Harmonic ACE Curved Shears
Intuitive Surgical recalls daVinci Harmonic ACE Curved Shears due to potential sterility breaches from damaged packaging during transit. Affected units may have pinholes or small openings in sterile pouches.
Intuitive SurgicalJan 16, 2019 - Lower riskMedical device
Intuitive Surgical, Inc. recalls Da Vinci Xi/X EndoWrist Monopolar Curved scissors (MCS), model number 470179-19, UDI: (00) 886874112298
Intuitive Surgical recalls Da Vinci Xi/X EndoWrist Monopolar Curved scissors (model 470179-19) due to potential failure to recognize monopolar energy in electrosurgical units, which could prevent proper surgical function.
Intuitive SurgicalDec 4, 2018 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci Xi Surgical System
Intuitive Surgical recalls da Vinci Xi surgical systems with a manufacturing variation causing persistent error 23087 that may lead to loss of arm functionality during surgery. Affected units include specific model and UDI numbers.
Intuitive SurgicalNov 21, 2018 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci SP Instrument Arm Drape. REF 430013-12 QTY 1 Pouch
Intuitive Surgical recalls da Vinci SP Instrument Arm Drape (REF 430013-12) due to potential tear during use, risking sterile barrier breaches. Affected units include all lots of this pouch.
Intuitive SurgicalOct 25, 2018 - Lower riskMedical device
Intuitive Surgical, Inc. recalls The da Vinci SP surgical system is made of three main components: the Surgeon Console (SC), the Vision Cart (VC), and
Intuitive Surgical recalls da Vinci SP surgical systems (models SP0022-SP0026) due to potential cannula mount button damage when released abruptly. Affected systems may require repair or replacement.
Intuitive SurgicalOct 23, 2018 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model No. 420179-16 Product Usage: EndoWrist Instruments,
Intuitive Surgical recalls da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model 420179-16 due to potential cracks in extension tube that could fracture and fall into patient during surgery.
Intuitive SurgicalAug 15, 2018 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci Si/X/Xi Surgical System Redundant Medical Grade Power Supply (RMGPS) Units The da Vinci System consists of a
Intuitive Surgical recalls specific Redundant Medical Grade Power Supply (RMGPS) units for da Vinci Si/X/Xi Surgical Systems due to potential failure during use, which could disrupt surgery. Affected units have model numbers listed in the recall notice.
Intuitive SurgicalJul 16, 2018 - Stop using nowMedical device
Intuitive Surgical, Inc. recalls EndoWrist Suction Irrigator, Single Use Instrument. Part Number: 480299-04. An accessory to the EndoWrist Surgical
Intuitive Surgical recalls EndoWrist Suction Irrigator (Part 480299-04) due to potential silicone particle generation during surgery, which could enter patients. Affected units include specific lots and part numbers.
Intuitive SurgicalJun 4, 2018 - Lower riskMedical device
Intuitive Surgical, Inc. recalls The da Vinci Xi Surgical System (IS4000) Model Name: IS4000, Endoscope Controller. Model Number: 372601-16.
Intuitive Surgical recalls da Vinci Xi Endoscope Controller (model IS4000) due to dim, color-imbalanced surgical images and potential fogging. Affected units have specific model and serial numbers.
Intuitive SurgicalMay 17, 2018 - Lower riskMedical device
Intuitive Surgical, Inc. recalls da Vinci Xi EndoWrist Stapler 45 Reload Green, Model 48445G-03, 12 reloads/box.
Intuitive Surgical recalls da Vinci Xi EndoWrist Stapler 45 Reload Green (Model 48445G-03) due to potential missing knife component causing failure to cut tissue. Affected units sold until 2020.
Intuitive SurgicalApr 23, 2018 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci X Surgical System, Model IS4200. Product Usage: The Intuitive Surgical Endoscopic Instrument Control System
Intuitive Surgical recalls da Vinci X Surgical System Model IS4200 with defective Arm Controller Joint (ACJ) boards that may fail, potentially causing system malfunctions during surgery.
Intuitive SurgicalMar 7, 2018 - Use cautionMedical device
Intuitive Surgical, Inc. recalls daVinci X EndoWrist(R) Stapler 45, REF 470298 Product Usage: The Intuitive Surgical EndoWrist Stapler 45, Stapler 45
Intuitive Surgical recalls daVinci X EndoWrist Stapler 45 models with serial numbers S10170630, S11170705, S10170707, S10170731 due to a potential manufacturing defect that may prevent the Stapler Release Kit Wrench from unclamping the instrument.
Intuitive SurgicalSep 19, 2017 - Use cautionMedical device
Intuitive Surgical, Inc. recalls da Vinci Xi Surgical System Product Usage: The da Vinci Xi Surgical System (IS4000) is designed to assist a surgeon in
Intuitive Surgical recalls da Vinci Xi Surgical System (IS4000) units with potentially under-torqued brake screws in patient side carts. This could cause system arm movement during surgery, risking patient injury. Affected units have specific serial numbers listed in the recall.
Intuitive SurgicalJun 1, 2017
Intuitive Surgical, Inc. recall questions
How many recalls has Intuitive Surgical, Inc. had?
106 recalls from Intuitive Surgical, Inc. are on record with U.S. safety agencies, from 2017–2026.
What is the most recent Intuitive Surgical, Inc. recall?
Intuitive Surgical, Inc. recalls Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000 Model/Catalog Number: 380746 Software Version: N/A Product, dated Apr 24, 2026. Every Intuitive Surgical, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Intuitive Surgical, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Intuitive Surgical, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.