Device recall

Z-1230-2007: 5mm x 30cm Hollow "Golf" Tip Ultrasonic Aspiration Probe, Model 5620-530…

FDA device recall · Class III · Mentor Texas, Inc

Key facts

Recall number (Z-number) Z-1230-2007
Recall event 38623
Product 5mm x 30cm Hollow "Golf" Tip Ultrasonic Aspiration Probe, Model 5620-530, Catalog Number 5620-530.
Product code MUU
Recalling firm Mentor Texas, Inc
Recall class Class III
Status Terminated
Termination date Apr 4, 2008
510(k) numbers K041058
FEI number 1000118360

At a glance

  • 1–9 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)