FDA recall record

Tecfen Medical 2.0mm Crescent Knife Angled Bevel Up recall — FDA Z-1954-2025

Sterility assurance for Ophthalmic knives.

Class IIclassification
Z-1954-2025official record ID
Jun 18, 2025report date

Recall record at a glance

Official recordZ-1954-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmTecfen Medical
Report dateJun 18, 2025
Recall initiation dateApr 25, 2025
Quantity42 units
LocationSanta Barbara, CA, United States

Official product description

Brand Name: Tecfen Medical Product Name: 2.0mm Crescent Knife Angled Bevel Up Model/Catalog Number: QKN1010 Software Version: No software Product Description: This is an ophthalmic knife (manual) that is to be sterile and packaged individually in Tyhvek 1059B. The crescent knife is used to create smooth, curved incisions for corneal transplant procedures, used in small incision cataract surgery and phacoemulsification to create self-sealing scleral tunnels, used for creating tunnel incisions in the sclera and cornea during procedures like trabeculectomy. Component: No

Why the product was recalled

Sterility assurance for Ophthalmic knives.

Distribution information

Worldwide - US Nationwide distribution in the states of Connecticut and Minnesota. The countries of Dominican Republic, Saudi Arabia, Mexico, Chile, Iran, South Africa, Honduras, UAE, Honduras, Qatar, Iran, and Bangladesh, Brazil and Israel.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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