FDA Device Intelligence
HomeDevice types › NKX

Needle, Phacoemulsification, Reprocessed

FDA product code NKX · Class 2 · Ophthalmic

27
Registered devices
12
Adverse events
11
Recalls
5
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2013-05-03Surgical Instrument Service And Savings, Inc.The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch.
2008-08-08Sterilmed IncSteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted becau
2008-03-26Bausch & Lomb IncThe directions for use are printed with the incorrect symbols to indicate the product is packaged as sterile and nonreusable
2008-03-26Bausch & Lomb IncThe directions for use are printed with the incorrect symbols to indicate the product is packaged as sterile and nonreusable
2008-03-26Bausch & Lomb IncThe directions for use are printed with the incorrect symbols to indicate the product is packaged as sterile and nonreusable
2008-03-26Bausch & Lomb IncThe directions for use are printed with the incorrect symbols to indicate the product is packaged as sterile and nonreusable
2008-03-26Bausch & Lomb IncThe directions for use are printed with the incorrect symbols to indicate the product is packaged as sterile and nonreusable
2008-03-26Bausch & Lomb IncThe directions for use are printed with the incorrect symbols to indicate the product is packaged as sterile and nonreusable
2008-03-26Bausch & Lomb IncThe directions for use are printed with the incorrect symbols to indicate the product is packaged as sterile and nonreusable
2008-03-26Bausch & Lomb IncThe directions for use are printed with the incorrect symbols to indicate the product is packaged as sterile and nonreusable

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.