Reported Jan 22, 2025 · Ongoing
8MM,LARGE HEM-O-LOK CLIP APPLIER,IS4000¿ REF 470230
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?
8MMLARGE HEM-O-LOK CLIP APPLIERIS4000¿ REF 470230
- Lot codes and dates
- Model Number470230
- Part Number470230-12
- UDI-DI code00886874112380
- Batch Numbers
84 of 84 codes
K10230103K10230122K10230123K10230212K10230226K10230302K10230310K10230315K10230323K10230405K10230420K10230427K10230504K10230511K10230518K10230525K10230602K10230608K10230615K10230622K10230706K10230713K10230727K10230803K10230810K10230817K10230921K10231005K10231012K10231019K10231027K10231109K10231123K10231130K10231207K10231214K10231218K10240119K10240125K10240208K10240215K10240222K10240229K10240307K10240327K10240404K10240411K10240418K10240516K10240523K10240606K10240620K10240627K10240702K10240711K10240718K10240808K10240822K11230103K11230108
- K12240404 K13230108 Model Number470230
- Part Number470230-14
- UDI-DI code00886874112380
- Batch NumbersK10230914
- Amount recalled
- 29,559
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 increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
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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