Reported Aug 28, 2024 · Ongoing
Product Desc: Product Name: 20 Gauge V-Lance Knife Model/Catalog Number: 8065912001 Software Version: N/A Product…
Alcon Research LLC
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: Alcon Research LLC · Aspex Facility · Fort Worth, TX · 76134-2099
Is this the product you have?
- Product DescProduct
- Name20 Gauge
- V-Lance Knife Model/Catalog Number8065912001
- Software VersionN/A
- Product DescriptionOphthalmic
- knife ComponentN/A
- Lot codes and dates
- Model/Catalog Number8065912001
- UDI-DI00380659120015
- Lot numbers
15W9CJ161A10161A2M163701164WWX16D4VU
- Amount recalled
- 39,954 units
This recall covers 36 products
The agency filed one notice per product. You are reading one of them; the other 35 are below.
23 more are in the archive.
Where it was sold
- Nationwide
- PR
Why it was recalled
Alcon has detected an increase in complaint reports related to sharpness for specific ClearCut Dual Bevel Sideport and A-OK Comeal/Scleral V-Lance Ophthalmic knives.
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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