Alcon Research LLC 2024-08-28 Health serious FDA
Health · FDA · Recall #FDA-Z-2664-2024
Product Desc: Product Name: CLEARCUT SB INTREPID 2.2 ANG Model/Catalog Number:… Recall
Issued August 28, 2024 · Alcon Research LLC
In August 2024, Alcon Research LLC recalled the Product Desc: Product Name: CLEARCUT SB INTREPID 2.2 ANG Model/Catalog Number:…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using Product Desc: Product Name: CLEARCUT SB INTREPID 2.2 ANG Model/Catalog Number:… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Alcon Research LLC to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Alcon Research LLC
- Category
- Health
- Recall date
- August 28, 2024
- Units affected
- Not reported
- Sold at
- Domestic: Nationwide Distribution Countries Affected: Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Colombia, Croat
- Recall number
- FDA-Z-2664-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Alcon Research LLC has 12 recalls in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.