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FDA (Device enforcement)Recalled 2024-07-15class ii

Alcon Research LLC: Product Desc: Product Name: CLEARCUT SB INTREPID 2.2 ANG Model/Catalog Number: 8065992445 Software Version: N/A Product Description: Ophthalmic knife Component: N/A

Hazard

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.

Details from the source

Reason for recall: 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. Distribution: Domestic: Nationwide Distribution Countries Affected: Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, China, Colombia, Croatia, Czech Republic, Denmark, Ecuador, Emirates, Finland, France, Germany, Greece, Hong Kong, Hungary, India, Ireland, Italy, Japan, Korea, Kosovo, Luxemburg, Malaysia, Mexico, Netherlands, New Zealand, Norway, Panama, Peru, Philippines, Poland, Portugal, Puerto Quantity: 35,199 units Lot/code info: Model/Catalog Number: 8065992445; UDI-DI: 00380659924453; Lot numbers: 169P2R, 16AV06, 16AV1Y, 16F1JU, 16K9HA, 167R42.

UPC codes

00380659924453

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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