Device recall

Z-1190-2008: Steris C1160 Universal Flexible Processing Tray, for use with STERIS SYSTEM 1…

FDA device recall · Class II · Steris Corp

Key facts

Recall number (Z-number) Z-1190-2008
Recall event 46753
Product Steris C1160 Universal Flexible Processing Tray, for use with STERIS SYSTEM 1 Processor, used for sterilization of flexible endoscopes.
Product code MED
Recalling firm Steris Corp
Recall class Class II
Status Terminated
Termination date Feb 24, 2012
510(k) numbers K875280
FEI number 1527821

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)