Device recall

Z-1008-2015: MAQUET Servo Humidifier 163; Model No.: 01-06-8125-8, catalog no…

FDA device recall · Class I · Teleflex, Inc.

Key facts

Recall number (Z-number) Z-1008-2015
Recall event 70127
Product MAQUET Servo Humidifier 163; Model No.: 01-06-8125-8, catalog no. XKC01-06-8125-8. A heat and moisture condenser (artificial nose) is a device intended to be positioned over a tracheotomy (a surgically created opening in the throat) or tracheal tube (a tube inserted into the trachea) to warm and…
Product code BYD
Recalling firm Teleflex, Inc.
Recall class Class I
Status Terminated
Termination date Mar 21, 2017
FEI number 3011369183

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)