Device recall

Z-0456-05: BacT/ALERT(BTA) Classic instruments.

FDA device recall · Class III · bioMerieux

Key facts

Recall number (Z-number) Z-0456-05
Recall event 30261
Product BacT/ALERT(BTA) Classic instruments.
Product code MDB
Recalling firm bioMerieux
Recall class Class III
Status Terminated
Termination date Dec 8, 2009
510(k) numbers K903505
FEI number 3002769706

At a glance

  • 1–9 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)