Device recall

Z-2015-2025: Servo-u MR Ventilator System. Model Number: 6888800.

FDA device recall · Class I · Maquet Critical Care AB

Key facts

Recall number (Z-number) Z-2015-2025
Recall event 97032
Product Servo-u MR Ventilator System. Model Number: 6888800.
Product code CBK
Recalling firm Maquet Critical Care AB
Recall class Class I
Status Open, Classified
510(k) numbers K201874
FEI number 3002808128

At a glance

  • 1–9 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)