Device recall

Z-2356-2011: Material DT9750, VAD ACCESS TRAY, CENTURION VAD ACCESS TRAY, REORDER DT9750…

FDA device recall · Class II · Centurion Medical Products Corporation

Key facts

Recall number (Z-number) Z-2356-2011
Recall event 58346
Product Material DT9750, VAD ACCESS TRAY, CENTURION VAD ACCESS TRAY, REORDER DT9750, STERILE, LATEX FREE, CENTURION MEDICAL PRODUCTS CORP. WILLIAMSTON MI 48895, USA 800.248.4058 www.centurionmp.com FACILITATES LINE INSERTION
Product code MCY
Recalling firm Centurion Medical Products Corporation
Recall class Class II
Status Terminated
Termination date Sep 13, 2011
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)