Reported Apr 8, 2026 · Ongoing
Brand Name: da Vinci S, Si Double Fenestrated Grasper Instrument Product Name: da Vinci S, Si Double Fenestrated…
Intuitive Surgical, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Intuitive Surgical, Inc. · 1266 Kifer Rd · Sunnyvale, CA · 94086-5304
Is this the product you have?
- Brand Nameda Vinci S, Si Double Fenestrated
- Grasper Instrument Product Nameda Vinci S, Si Double Fenestrated
- Grasper Instrument Model/Catalog Number420189
- Software VersionNA
- Product DescriptionEndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp endoscopic dissectors, scissors, scalpels, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories are intended for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, suturing, and delivery and placement of microwave and cryogenic ablation probes and accessories. Please refer to attached User Manual for additional details on intended use. All da Vinci S/Si reusable instruments with jaws use mechanical tungsten cables and pulleys to transmit motion from the input discs to the housing (on the proximal chassis), through the main shaft, and the distal instrument tip (inside the patient)
- ComponentNA
- Lot codes and dates
- Lot Code420189
- Double Fenestrated Grasper GTIN00886874111581
- FDA Medical Device Listing NumberD088920
- Material Number420189-07
- Batch / System Numbers
129 of 129 codes
M10120911SH1182M10130103SH1182M10130116SH1182M10130124SH1182M10130422SH1182M10130731SH1182M10130918SH1182M10110112SG704M10110202SG704M10110318SG704M10111028SG704M20111221SG704M10120220SG704M10120419SG704M10130110SG704M10130422SG704M10130726SG704M10130802SG704M10130802SH0547M10130918SH0547M10110808SH0059M10111027SH0059M10111104SH0059M10121123SH0059M10121213SH0059M10130103SH0059M10130815SH1557M10130625SH1390M10130731SH1390M10130802SH1390
- USG518 M10130829 USG518 Material Number420189-09
- Batch / System Numbers
225 of 225 codes
M10131104SH1182M10140228SH1182M10140414SH1182N10140508SH1182N10140619SH1182N10140703SH1182N10140812SH1182N10140902SH1182N10141204SH1182N10150430SH1182N10150814SH1182N10150916SH1182N10151106SH1182N10151119SH1182N10160429SH1182N10160520SH1182N10150825SH1182N10160617SH1182N10160914SH1182N10161012SH1182N10161222SH1182N10160908SH1182N10180105SH1182N10140521SG704N10140801SG704N10141017SG704N10150309SG704N10150526SG704N10150805SG704N10160106SG704
- SH1276 N10150129 USG518 Material Number420189-10
- Batch / System Numbers
N10180409SH1182N10180702SH1182N10180509SG704N10180223SH1557N10180712SH1557N12180123
- SH0825 N10180409 SH1279 Material Number420189-11
- Batch / System Numbers
N10190128SH1182N10190206SH1182N10180814SH1557N10181005SH1557N10180802SH1557N10180928SH1557N10190423SH1557N10190902SH1557N10180814SH0825N10190805SH0825N10190306SH2180N10190128
- SH1604 N10180814 SH2144 Material Number420189-12
- Batch / System Numbers
N10190715SH1182N10190502SH1182N10190513SH1182N10190513SH1557N10190408SH1557N10190715SH1557N10200217SH1557N10200803SH1557N10201005SH1557N10210419SH1557N10210210SH1557N10200217SH1964N10200720SH1964N10200427SH1964N10210419SH1964N10210308SH1964N10210713SH1964N10200427SH1604N10210104SH1604N10190502SH1385N10210913SH2144K10220925SH2144K10231026SH2144
- Amount recalled
- 2370
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
Why it was recalled
Due to increased complaints for broken/frayed grip cables for reusable instruments.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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