Device recall

Z-0915-2013: AMSCO C and AMSCO 400 Steam Sterilizers designed for sterilization of heat and…

FDA device recall · Class II · Steris Corporation

Key facts

Recall number (Z-number) Z-0915-2013
Recall event 64440
Product AMSCO C and AMSCO 400 Steam Sterilizers designed for sterilization of heat and moisture-stable materials used in healthcare facilities.
Product code FLE
Recalling firm Steris Corporation
Recall class Class II
Status Terminated
Termination date Dec 5, 2013
510(k) numbers K111223, K112403
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

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