Device recall

Z-1065-2020: Centurion-Incision /Drainage Tray ID1235A ESKENAZI INCISION & DRAINAGE TRAY…

FDA device recall · Class II · Centurion Medical Products Corporation

Key facts

Recall number (Z-number) Z-1065-2020
Recall event 84530
Product Centurion-Incision /Drainage Tray ID1235A ESKENAZI INCISION & DRAINAGE TRAY ID1525 INCISION & DRAINAGE TRAY ID1670 I&D TRAY ID1715 INCISION & DRAINAGE TRAY ID1765 ER I&D PACK ID1765 ER I&D PACK ID1835 I & D TRAY ID2075 I&D TRAY ID585 INCISION & DRAINAGE TRAY ID875 INCISION & DRAINAGE TRAY ID875…
Product code LRP
Recalling firm Centurion Medical Products Corporation
Recall class Class II
Status Terminated
Termination date Sep 4, 2020
FEI number 3008403546

At a glance

  • None Linked 510(k)s
  • 10–99 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)