Reported Apr 8, 2026 · Ongoing
Brand Name: da Vinci S, Si Grasping Retractor Instrument Product Name: da Vinci S, Si Grasping Retractor Instrument…
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 Grasping
- Retractor Instrument Product Nameda Vinci S, Si Grasping Retractor
- Instrument Model/Catalog Number420278
- 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 Code420278:
- Grasping Retractor GTIN00886874111772
- FDA Medical Device Listing NumberD088920
- Material Number420278-04
- Batch / System Numbers
65 of 65 codes
M10110613SH1182M10120127SH1182M10120217SH1182M10120829SH1182M10130103SH1182M10130114SH1182M11130404SH1182M10130527SH1182M10130606SH1182M10130909SH1182M10130925SH1182S10101229SG704S10110105SG704M10121214SH0547M10110118SH0059M10110613SH0059S10110819SH0059M10121122SH0059M10121214SH0059M10130114SH0059M10130220SH0059M10130319SH0059M11130404SH0059M10120912SH1390M10130730USG721M10130909USG721M10110307SH0729M10130214SH0729M11130404SH0729M10130617SH0729
- SH1279 M10111028 SH0761 Material Number420278-06
- Batch / System Numbers
127 of 127 codes
M10140115SH1182N10140725SH1182N10140923SH1182N10150324SH1182N10150417SH1182N10150721SH1182N10150608SH1182N10150820SH1182N10151113SH1182N10151214SH1182N10151029SH1182N10160304SH1182N10151201SH1182N10141205SH1182N10160921SH1182N10161123SH1182N10170516SH1182N10170601SH1182N10170921SH1182N10171213SH1182N10171226SH1182N10180417SH1182N10140815SG704N10150210SG704N10150608SG704N10160203SG704N10170117SG704N10170921SG704N10170822SG704N10171002SG704
- SH1385 N10171117 SH1385 Material Number420278-07
- Batch / System Numbers
N10181219SH1182N10180906SH1182N10190423SH1182N10181114SH1182N10180906SG704N10180910
- USG721 N10181114 SH1604 Material Number420278-09
- Batch / System Numbers
N10190826SH1182N10190515SH1182N10190909SH1182N10190902SH1964N10190826SH1964N10190515SH1964N10190909SH1964N10190826USG721N10190902SH1604
- Amount recalled
- 2660
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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