CLASS II ONGOING Device recall · Reported 18 Jun 2025 · FDA Enforcement Report

Slit Knife, Angled recalled by Tecfen Medical

Tecfen Medical is recalling Slit Knife, Angled, distributed nationwide in the US. The recall was initiated on 25 Apr 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Code: Manufacture date: 2024-11-21 Expiration date: 2027-11-20 Lot number: ZGY24081907-02 UDI: 00817618021156
Quantity recalled115 unit

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-1951-2025
FDA event ID
96872
Recalling firm
Tecfen Medical, Santa Barbara, CA
Classification
Class II
Status
Ongoing
Recall initiated
25 Apr 2025
FDA classified
11 Jun 2025
Reported
18 Jun 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility
Device type
Medical Software

Timeline

25 Apr 2025Recall initiated by company
11 Jun 2025Classified by FDA+47 days
18 Jun 2025Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Sterility assurance for Ophthalmic knives.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

Brand Name: Tecfen Medical Product Name: 2.4mm Slit Knife, Angled Model/Catalog Number: QKN2461 Software Version: No software Product Description: This is an ophthalmic knife (manual) that is to be sterile (gamma radiation) and packaged individually in Tyvek 1059B. Slit knives are used to create precise incisions for controlled entry into the eye. Component: No

Where it was distributed

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.

Nationwide ConnecticutMinnesota

Questions about this recall

Why was it recalled?

Sterility assurance for Ophthalmic knives.

Which lots are affected?

Lot Code: Manufacture date: 2024-11-21 Expiration date: 2027-11-20 Lot number: ZGY24081907-02 UDI: 00817618021156

Where was it sold?

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.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

6 other products · FDA event 96872

This product is part of a recall event; the main page for the event is Slit Knife, Angled recalled by Tecfen Medical.

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