Device recall

Z-0933-2008: Linemaster Wireless Footswitch Accessory, Model SP-9970214-005112010 and Model…

FDA device recall · Class II · Sound Surgical Technologies, LLC

Key facts

Recall number (Z-number) Z-0933-2008
Recall event 46293
Product Linemaster Wireless Footswitch Accessory, Model SP-9970214-005112010 and Model SP-9970214-005112232. Sound Surgical Technologies, LLC, Louisville, CO 80027.
Product code GEI
Recalling firm Sound Surgical Technologies, LLC
Recall class Class II
Status Terminated
Termination date Apr 1, 2008
510(k) numbers K022051, K991791, K993868
FEI number 3004106598

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)