Device recall

Z-1139-2008: AMO VISX STAR Excimer Laser System, manufactured by VISX, Santa Clara, CA 95051

FDA device recall · Class II · VISX INCORPORATED, A SUBSIDIARY OF AMO INC

Key facts

Recall number (Z-number) Z-1139-2008
Recall event 46393
Product AMO VISX STAR Excimer Laser System, manufactured by VISX, Santa Clara, CA 95051
Product code LZS
Recalling firm VISX INCORPORATED, A SUBSIDIARY OF AMO INC
Recall class Class II
Status Terminated
Termination date May 5, 2010
PMA numbers P930016
FEI number 1221842

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 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)