Reported Jan 22, 2025 · Ongoing

8MM, Tenaculum Forceps REF 470207 Instrument used with the da Vinci X/Xi Surgical Systems in a wide variety of…

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?

  • 8MM, Tenaculum Forceps REF 470207 Instrument used with the da Vinci X/Xi Surgical Systems in a wide variety of procedures to perform a variety of surgical tasks including manipulation and retraction of tissue.
Lot codes and dates
  • Product Number470207
  • UDI-Di code00886874112366
  • Part Number and Version470207-04
  • Lot NumbersS10131217
  • S10131218 Part Number and Version470207-07
  • Lot Numbers
    • S10140619
    • S10140622
    • S10140626
    • S10140718
    • S10140811
    • S10140912
    • S10141113
    • S10141121
    • S10150117
  • S10150202 Part Number and Version470207-08
  • Lot Numbers

    98 of 98 codes

    • N10160112
    • N10160128
    • N10160219
    • N10160316
    • N10160407
    • N10160420
    • N10160629
    • N10160705
    • N10160802
    • N10160824
    • N10160830
    • N10160914
    • N10160929
    • N10161011
    • N10161103
    • N10161109
    • N10161129
    • N10161212
    • N10170111
    • N10170201
    • N10170217
    • N10170308
    • N10170410
    • N10170509
    • N10170517
    • N10170612
    • N10170623
    • N10170705
    • N10170720
    • N10170809
    • N10170821
    • N10170829
    • N10170908
    • N10170927
    • N10171123
    • N10171204
    • N10180108
    • N10180119
    • N10180307
    • N10180308
    • N10180322
    • N10180404
    • N10180423
    • N10180516
    • N10180523
    • N10180528
    • N10180605
    • N10180613
    • S10141219
    • S10150207
    • S10150213
    • S10150310
    • S10150401
    • S10150416
    • S10150505
    • S10150518
    • S10150520
    • S10150618
    • S10150707
    • S10150715
  • T10180213 Part Number and Version470207-10
  • Lot Numbers

    191 of 191 codes

    • K10210726
    • K10210921
    • K10210927
    • K10211004
    • K10211011
    • K10211018
    • K10211025
    • K10211108
    • K10211116
    • K10211122
    • K10211129
    • K10211213
    • K10211220
    • K10220117
    • K10220214
    • K10220228
    • K10220307
    • K10220314
    • K10220321
    • K10220425
    • K10220502
    • K10220523
    • K10220530
    • K10220606
    • K10220613
    • K10220620
    • K10220704
    • K10220711
    • K10220718
    • K10220725
    • K10220802
    • K10220808
    • K10220815
    • K10220905
    • K10220926
    • K10221009
    • K10221016
    • K10221030
    • K10221102
    • K10221212
    • K10221218
    • K10230108
    • K10230205
    • K10230212
    • K10230226
    • K10230302
    • K10230310
    • K10230316
    • K10230323
    • K10230420
    • K10230427
    • K10230504
    • K10230511
    • K10230518
    • K10230525
    • K10230601
    • K10230608
    • K10230615
    • K10230706
    • K10230713
Amount recalled
33,219

This recall covers 39 products

The agency filed one notice per product. You are reading one of them; the other 38 are below.

26 more are in the archive.

Where it was sold

Why it was recalled

Due to an increase in complaints for pitch cable failures related to forceps and small Graptor instruments

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:00 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.