Device recall

Z-2073-2014: LP,Surgical Fibers, Bare Laser Fiber 600 micron, DBLF-60-2, Sterile EO. Laser…

FDA device recall · Class II · Laser Peripherals LLC

Key facts

Recall number (Z-number) Z-2073-2014
Recall event 68674
Product LP,Surgical Fibers, Bare Laser Fiber 600 micron, DBLF-60-2, Sterile EO. Laser surgical instrument for use in general and plastic surgery and in dermatology
Product code GEX
Recalling firm Laser Peripherals LLC
Recall class Class II
Status Terminated
Termination date Oct 22, 2014
510(k) numbers K030959
FEI number 1221543

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 100–999 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

Browse all FDA device recalls (products)