Device recall

Z-1519-2020: Custom procedure trays containing medical components needed to facilitate…

FDA device recall · Class II · Avid Medical, Inc.

Key facts

Recall number (Z-number) Z-1519-2020
Recall event 85049
Product Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgeries. Multiple item and lot numbers.
Product code OGJ
Recalling firm Avid Medical, Inc.
Recall class Class II
Status Terminated
Termination date Nov 23, 2020
FEI number 1047429

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)