Reported Aug 28, 2024 · Ongoing
Product Desc: Product Name: CLEARCUT SATINSLIT FULL HANDLE2.75MM AN Model/Catalog Number: 8065992745 Software Version:…
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
- NameCLEARCUT SATINSLIT FULL HANDLE2.75MM
- AN Model/Catalog Number8065992745
- Software VersionN/A
- Product DescriptionOphthalmic
- knife ComponentN/A
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Barcodes Product as published 8065992745Model/ — 00380659927454UDI-DI: 00380659927454 — Lot numbers: 15X55P, 161A1C, 162WXV, 162WXW, 162WXX, 1636Y1, 1668MJ, 1668MK, 167R2Y, 168UEV, 16DFK6, 16DFXL, 16DNHY, 16EV4J, 16EV4K, 16F1PT, 16FXNX, 16FXNY, 16H1K6, 16J7UC, 1668NN, 169P3F, 16AM3T, 16AV0F, 16DFY9, 16EV4N. - Amount recalled
- 145,248 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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