Device recall

Z-2629-2011: Servo-s Ventilator Systems; Article number 66 40 440. Intended for treatment and…

FDA device recall · Class II · Maquet Inc.

Key facts

Recall number (Z-number) Z-2629-2011
Recall event 58793
Product Servo-s Ventilator Systems; Article number 66 40 440. Intended for treatment and monitoring of patients in the range of neonates, infants and adults with respiratory insufficiency; these are only to be used by healthcare providers in hospitals or healthcare facilities and for in-hospital transport…
Product code CBK
Recalling firm Maquet Inc.
Recall class Class II
Status Terminated
Termination date Sep 17, 2013
FEI number 3008355164

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

Browse all FDA device recalls (products)