Reported Jan 22, 2025 · Ongoing
8MM, Small Graptor REF 470318 Is a grasping retractor Instrument used with the da Vinci X/Xi Surgical Systems in a wide…
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, Small Graptor REF 470318 Is a grasping retractor 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 Number470318
- UDI-Di code00886874112441
- Part Number and Version470318-04
- Lot NumbersS10131209
- S10131210 Part Number and Version470318-07
- Lot Numbers
S10140617S10140618S10140619S10140620S10140717S10140801S10140812S10140821S10140823S10140915S10141008S10141120S10141205S10141219S10150108S10150120S10150122S10150206S10150212
- S11140620 Part Number and Version470318-08
- Lot Numbers
127 of 127 codes
N10151230N10160104N10160113N10160203N10160218N10160219N10160307N10160317N10160330N10160404N10160406N10160420N10160426N10160525N10160607N10160616N10160725N10160726N10160802N10160810N10160824N10160901N10160914N10160927N10161010N10161020N10161102N10161111N10161128N10161209N10170119N10170203N10170222N10170309N10170330N10170419N10170502N10170512N10170518N10170612N10170623N10170703N10170725N10170728N10170801N10170802N10170822N10170823N10170906N10170914N10171012N10171101N10171115N10171124N10171206N10171219N10171227N10180122N10180131N10180209
- T10171127 Part Number and Version470318-10
- Lot Numbers
206 of 206 codes
K10210921K10210927K10211004K10211011K10211018K10211103K10211108K10211116K10211117K10211122K10211206K10211213K10220217K10220221K10220228K10220307K10220314K10220404K10220425K10220511K10220516K10220613K10220725K10220802K10220808K10220815K10220912K10220926K10221016K10221030K10221102K10221106K10221113K10221117K10221118K10230212K10230219K10230226K10230420K10230504K10230511K10230518K10230525K10230601K10230608K10230615K10230706K10230713K10230803K10230817K10230831K10230907K10230914K10230921K10230928K10231012K10231019K10231027K10231130K10231207
- Amount recalled
- 42028 devices
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.
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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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