Device recall

Z-1154-06: Stericover/ Sterile Disposible Polyethylene Drape ---Universal Video Camera/…

FDA device recall · Class II · Abbott Spine

Key facts

Recall number (Z-number) Z-1154-06
Recall event 35508
Product Stericover/ Sterile Disposible Polyethylene Drape ---Universal Video Camera/ Laser Arm Equipment Cover; 7'' x 96''.
Product code KKX
Recalling firm Abbott Spine
Recall class Class II
Status Terminated
Termination date Sep 25, 2007
FEI number 3000718496

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)