Data Foundry

Medical device recalls 2025

Brand Name: Tecfen Medical Product Name: 2 — Class II medical device recall Z-1954-2025

Ongoing recall by Tecfen Medical, reported 2025-06-18, distributed nationwide. Sterility assurance for Ophthalmic knives.

Recall numberZ-1954-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmTecfen Medical, Santa Barbara, CA, United States
Recall initiated2025-04-25
Classified2025-06-11
Reported by FDA2025-06-18
DistributedNationwide (US)
Countries outside the USAE, BD, BR, CL, DO, HN, IL, IR, MX, QA, SA, ZA
Quantity42 units
Reason classessterility
UPC / GTIN / UDI-DI00817618021330
Lot numbersZGY24071501-03
Model numbersQKN1010
Expiration dates2027-11-21

Product

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

Reason for recall

Sterility assurance for Ophthalmic knives.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1954-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.