--- title: "Intuitive Surgical, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Intuitive Surgical, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/intuitive-surgical-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Intuitive Surgical, Inc. recall records **69** reported ongoing 72 records in this archive. Latest source date Apr 24, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Apr 24, 2026 FDA device enforcement ### [Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000 Model/Catalog Number: 380746 Software Version: N/A Product Description: Preface: This report under 21 CFR 806.10 is be...](https://isitonrecall.com/recall/fda-device-z-2310-2026-brand-name-da-vinci-5-product-name-assy-dv5-tower-is5000-model-catalog-number-380746-software-versio/) Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching from the handheld camera to the robotic endoscope. Class II Reported ongoing Distribution: U.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NE, NH, NJ, NM, NV, NY, NC, ND, OH, OK, OR, PA, PR, SC, SD, TN, TX, UT,... [Official source for Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000 Model/Catalog Number: 380746 Software ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2310-2026%22) Apr 22, 2026 FDA device enforcement ### [Da Vinci ASSY, PSS, SP1098, Part Number: 380601](https://isitonrecall.com/recall/fda-device-z-2521-2026-da-vinci-assy-pss-sp1098-part-number-380601/) Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would prevent E-brake engagement and may result in uncontrolled motion. In addition, if it moves/backs ou... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of CA, GA, OH, PA, NY, MN, TN, OR, IL, MD, NJ, AL, NV, TX, FL, LA, CT, NC, AZ, IA, MO, WA, MI, WV, WI, KY, KS, VA,... [Official source for Da Vinci ASSY, PSS, SP1098, Part Number: 380601](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2521-2026%22) Apr 2, 2026 FDA device enforcement ### [Brand Name: Da Vinci X and Da Vinci Xi Product Name: da Vinci X, Xi Surgical System Model/Catalog Number: IS4000; IS4200 Software Version: N/A Product Description: he da Vinci X...](https://isitonrecall.com/recall/fda-device-z-2046-2026-brand-name-da-vinci-x-and-da-vinci-xi-product-name-da-vinci-x-xi-surgical-system-model-catalog-numbe/) Due to manipulator containing screws with in the arm sub-assembly that my be susceptible to breaking. Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, N... [Official source for Brand Name: Da Vinci X and Da Vinci Xi Product Name: da Vinci X, Xi Surgical System Model/Catalog...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2046-2026%22) Mar 11, 2026 FDA device enforcement ### [Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06](https://isitonrecall.com/recall/fda-device-z-1855-2026-intuitive-8-mm-sureform-30-gray-reloads-reference-numbers-48230m-05-and-48230m-06/) Reloads for curved-tipped stapler may potentially produce an incomplete staple line. Class I Reported ongoing Distribution: US: Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware District of Columbia Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Ma... [Official source for Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1855-2026%22) Dec 30, 2025 FDA device enforcement ### [da Vinci 5 Surgeon Console Viewer Display, ASSY, DV5 CONSOLE, IS5000, Part Number: 380730-45](https://isitonrecall.com/recall/fda-device-z-1355-2026-da-vinci-5-surgeon-console-viewer-display-assy-dv5-console-is5000-part-number-380730-45/) Robotic-assisted surgical system has Viewer Display manufactured with outdated firmware, may result in loss of one display-loss of 3D surgical field (depth perception) but 2D maintained, or loss of both displays-complete visualization loss, without fault, i... Class II Reported ongoing Distribution: US Nationwide distribution in the states of KS, AZ, MA, FL, MI, NC, IL, DC, TX, KY, MS, CA, MN, NV, NY, WI, ID, GA, CT, SC, UT, VA. [Official source for da Vinci 5 Surgeon Console Viewer Display, ASSY, DV5 CONSOLE, IS5000, Part Number: 380730-45](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1355-2026%22) Dec 15, 2025 FDA device enforcement ### [da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073 (2.7-4cm,SP1098, Box) & 430075 (2.7-7cm,SP1098,Box)](https://isitonrecall.com/recall/fda-device-z-1096-2026-da-vinci-sp-sp-access-port-kit-large-incision-reference-numbers-430073-2-7-4cm-sp1098-box-430075-2-7/) Access Port System tray may develop cracks potentially resulting in a sterility breach. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of Alabama, Arizona, California, Colorado, Connecticut, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentuck... [Official source for da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073 (2.7-4cm,SP1098, Box) & ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1096-2026%22) Dec 9, 2025 FDA device enforcement ### [Brand Name: da Vinci S, Si Monopolar Curved Scissors Instrument Product Name: da Vinci S and Si Monopolar Curved Scissors Instrument Model/Catalog Number: 420179 Software Versio...](https://isitonrecall.com/recall/fda-device-z-1696-2026-brand-name-da-vinci-s-si-monopolar-curved-scissors-instrument-product-name-da-vinci-s-and-si-monopol/) Due to increased complaints for broken/frayed grip cables for reusable instruments. Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution in the states of CA, FL, GA, IA, IL, IN, KS, KY, LA, MA, MO, MS, NC, NJ, NY, OH, PA, TX, VA and WI. The countries of Argentina, Brazil, ... [Official source for Brand Name: da Vinci S, Si Monopolar Curved Scissors Instrument Product Name: da Vinci S and Si M...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1696-2026%22) Dec 9, 2025 FDA device enforcement ### [Brand Name: da Vinci S, Si Double Fenestrated Grasper Instrument Product Name: da Vinci S, Si Double Fenestrated Grasper Instrument Model/Catalog Number: 420189 Software Version...](https://isitonrecall.com/recall/fda-device-z-1697-2026-brand-name-da-vinci-s-si-double-fenestrated-grasper-instrument-product-name-da-vinci-s-si-double-fen/) Due to increased complaints for broken/frayed grip cables for reusable instruments. Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution in the states of CA, FL, GA, IA, IL, IN, KS, KY, LA, MA, MO, MS, NC, NJ, NY, OH, PA, TX, VA and WI. The countries of Argentina, Brazil, ... [Official source for Brand Name: da Vinci S, Si Double Fenestrated Grasper Instrument Product Name: da Vinci S, Si Dou...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1697-2026%22) Dec 9, 2025 FDA device enforcement ### [Brand Name: da Vinci S, Si Mega Needle Driver Instrument Product Name: da Vinci S, Si Mega Needle Driver Instrument Model/Catalog Number: 420194 Software Version: NA Product Des...](https://isitonrecall.com/recall/fda-device-z-1698-2026-brand-name-da-vinci-s-si-mega-needle-driver-instrument-product-name-da-vinci-s-si-mega-needle-driver/) Due to increased complaints for broken/frayed grip cables for reusable instruments. Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution in the states of CA, FL, GA, IA, IL, IN, KS, KY, LA, MA, MO, MS, NC, NJ, NY, OH, PA, TX, VA and WI. The countries of Argentina, Brazil, ... [Official source for Brand Name: da Vinci S, Si Mega Needle Driver Instrument Product Name: da Vinci S, Si Mega Needle...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1698-2026%22) Dec 9, 2025 FDA device enforcement ### [Brand Name: da Vinci S, Si Grasping Retractor Instrument Product Name: da Vinci S, Si Grasping Retractor Instrument Model/Catalog Number: 420278 Software Version: NA Product Des...](https://isitonrecall.com/recall/fda-device-z-1699-2026-brand-name-da-vinci-s-si-grasping-retractor-instrument-product-name-da-vinci-s-si-grasping-retractor/) Due to increased complaints for broken/frayed grip cables for reusable instruments. Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution in the states of CA, FL, GA, IA, IL, IN, KS, KY, LA, MA, MO, MS, NC, NJ, NY, OH, PA, TX, VA and WI. The countries of Argentina, Brazil, ... [Official source for Brand Name: da Vinci S, Si Grasping Retractor Instrument Product Name: da Vinci S, Si Grasping Re...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1699-2026%22) Dec 9, 2025 FDA device enforcement ### [Brand Name: da Vinci S, Si Tenaculum Forceps Instrument Product Name: da Vinci S, Si Tenaculum Forceps Instrument Model/Catalog Number: 420207 Software Version: N/A Product Desc...](https://isitonrecall.com/recall/fda-device-z-1700-2026-brand-name-da-vinci-s-si-tenaculum-forceps-instrument-product-name-da-vinci-s-si-tenaculum-forceps-i/) Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments Class II Reported ongoing Distribution: U.S. Nationwide distribution in the states of AR, CA, CT, FL, IA, IL, IN, KS, KY, LA, MA, MD, MN, MO, MS, NJ, NM, NY, NC, OH, PA, TX, VA, and WA. The countries of Argentina, Aus... [Official source for Brand Name: da Vinci S, Si Tenaculum Forceps Instrument Product Name: da Vinci S, Si Tenaculum Fo...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1700-2026%22) Dec 9, 2025 FDA device enforcement ### [Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument Product Name: da Vinci S, Si Permanent Cautery Hook Instrument Model/Catalog Number: 420183 Software Version: NA Pro...](https://isitonrecall.com/recall/fda-device-z-1701-2026-brand-name-da-vinci-s-si-permanent-cautery-hook-instrument-product-name-da-vinci-s-si-permanent-caut/) Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments Class II Reported ongoing Distribution: U.S. Nationwide distribution in the states of AR, CA, CT, FL, IA, IL, IN, KS, KY, LA, MA, MD, MN, MO, MS, NJ, NM, NY, NC, OH, PA, TX, VA, and WA. The countries of Argentina, Aus... [Official source for Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument Product Name: da Vinci S, Si Permane...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1701-2026%22) Dec 4, 2025 FDA device enforcement ### [Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog Number: 490127 Software Version: N/A Product Description: The Ion Endoluminal System is a rob...](https://isitonrecall.com/recall/fda-device-z-1134-2026-brand-name-ion-endoluminal-system-product-name-ion-vision-probe-bag-model-catalog-number-490127-soft/) Due to probe bags that may have a compromised or incomplete sterile pouch seal. Class II Reported ongoing Distribution: U.S.: AL, AK, AZ, AR, CA, CO, CT, DE, DC, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MA, MD, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN,... [Official source for Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog Number: 49012...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1134-2026%22) Nov 17, 2025 FDA device enforcement ### [Da Vinci 5 ASSY, DV5 CONSOLE, IS5000 Model/Catalog Number: 380730 Used for minimally invasive surgery.](https://isitonrecall.com/recall/fda-device-z-1428-2026-da-vinci-5-assy-dv5-console-is5000-model-catalog-number-380730-used-for-minimally-invasive-surgery/) 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. Class II Reported ongoing Distribution: US distribution: LA, MA, NY, PA, TX, and VA. [Official source for Da Vinci 5 ASSY, DV5 CONSOLE, IS5000 Model/Catalog Number: 380730 Used for minimally invasive sur...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1428-2026%22) Nov 7, 2025 FDA device enforcement ### [Brand Name: Da Vinci Product Name: da Vinci X, Xi Surgical System, & da Vinci 5 Surgical System Model/Catalog Number: IS4000; IS4200; IS5000 Software Version: N/A Product Descri...](https://isitonrecall.com/recall/fda-device-z-1232-2026-brand-name-da-vinci-product-name-da-vinci-x-xi-surgical-system-da-vinci-5-surgical-system-model-cata/) Due to a software implementation error that allowed instruments arms failing an important diagnostic test to remain in clinical use. This test was supposed to be used to detect Universal Surgical Manipulator insertion axis ball screws that exhibit the sympt... Class II Reported ongoing Distribution: U.S.: AL, AR, CA, CO, CT, FL, ID, IL, IN, KS, KY, MD, MI, MN, MS, MO, NC, NJ, NV, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA, and WI. O.U.S.: Austria, Brazil, China, France, Germany... [Official source for Brand Name: Da Vinci Product Name: da Vinci X, Xi Surgical System, & da Vinci 5 Surgical System M...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1232-2026%22) May 12, 2025 FDA device enforcement ### [da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15](https://isitonrecall.com/recall/fda-device-z-2722-2026-da-vinci-sp-instrument-arm-drape-sp-1-pack-part-number-430013-13-430013-15/) Robotic-assisted surgical system arm drapes may detach from the instrument arm due to an issue involving the drape rings located at the top of the product, which may expose a section of instrument arm, which may result in procedure delay or conversion to an... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of NJ, OR, NY, FL, AL, SD, TX, VA, WV, PA, CA, WA, CT, MA, IL, OK, OH, MI, NC, MO, KY, WI, AZ, CO, GA, MD, SC, IN, NV, TN, M... [Official source for da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2722-2026%22) Feb 26, 2025 FDA device enforcement ### [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...](https://isitonrecall.com/recall/fda-device-z-1325-2025-brand-name-da-vinci-5-product-name-assy-dv5-console-is5000-foot-tray-pedals-model-catalog-number-380/) Due to an increase in complaints concerning foot tray pedal spring failing resulting in the pedal remaining pressed Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Alaska, Arizona, Arkansas, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Idaho, Illinois... [Official source for Brand Name: Da Vinci 5 Product Name: ASSY,DV5 CONSOLE,IS5000 Foot Tray Pedals Model/Catalog Numbe...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1325-2025%22) Dec 19, 2024 FDA device enforcement ### [8MM, MONOPOLAR CURVED SCISSORS, IS4000 REF 470179](https://isitonrecall.com/recall/fda-device-z-0847-2025-8mm-monopolar-curved-scissors-is4000-ref-470179/) Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws. Class II Reported ongoing Distribution: U.S. - Nation-wide. Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Io... [Official source for 8MM, MONOPOLAR CURVED SCISSORS, IS4000 REF 470179](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0847-2025%22) Dec 19, 2024 FDA device enforcement ### [8MM, POTTS SCISSORS, IS4000 REF 470001](https://isitonrecall.com/recall/fda-device-z-0848-2025-8mm-potts-scissors-is4000-ref-470001/) Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws. Class II Reported ongoing Distribution: U.S. - Nation-wide. Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Io... [Official source for 8MM, POTTS SCISSORS, IS4000 REF 470001](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0848-2025%22) Dec 19, 2024 FDA device enforcement ### [8MM, LARGE NEEDLE DRIVER, IS4000 REF 470006](https://isitonrecall.com/recall/fda-device-z-0849-2025-8mm-large-needle-driver-is4000-ref-470006/) Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws. Class II Reported ongoing Distribution: U.S. - Nation-wide. Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Io... [Official source for 8MM, LARGE NEEDLE DRIVER, IS4000 REF 470006](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0849-2025%22) ## Reasons in these listed records - Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching from the handheld camera to the robotic endoscope. - Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would prevent E-brake engagement and may result in uncontrolled motion. In addition, if it moves/backs out it may cause restr... - Due to manipulator containing screws with in the arm sub-assembly that my be susceptible to breaking. - Reloads for curved-tipped stapler may potentially produce an incomplete staple line. These examples come from this result page and are not a ranking of every recall reason. ## Checking Intuitive Surgical, Inc. ### Is there a recall on intuitive surgical, inc. right now? This archive contains 72 records, including 69 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Intuitive Surgical, Inc.](https://isitonrecall.com/check/?q=Intuitive%20Surgical%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)