Device recall

Z-0606-2014: RTC 25-C Inline Aerosol Tee Adapter. Intended to be used to adapt an aerosolized…

FDA device recall · Class II · Instrumentation Industries Inc

Key facts

Recall number (Z-number) Z-0606-2014
Recall event 66902
Product RTC 25-C Inline Aerosol Tee Adapter. Intended to be used to adapt an aerosolized medication delivery system having an elliptical mouthpiece to a ventilator circuit.
Product code CAI
Recalling firm Instrumentation Industries Inc
Recall class Class II
Status Terminated
Termination date Jul 9, 2014
FEI number 2518436

At a glance

  • None 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

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