Device recall

Z-0544-2020: Accessory kit, Alinity i containing Alinity ci Level Sensor, Bulk Solution

FDA device recall · Class II · Abbott Gmbh & Co. KG

Key facts

Recall number (Z-number) Z-0544-2020
Recall event 83847
Product Accessory kit, Alinity i containing Alinity ci Level Sensor, Bulk Solution
Product code JJE
Recalling firm Abbott Gmbh & Co. KG
Recall class Class II
Status Open, Classified
FEI number 3002809144

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)