Device recall

Z-2886-2011: ***** EXPANDED RECALL ***** Rusch Foley Catheter Insertion Tray with…

FDA device recall · Class II · Teleflex Medical

Key facts

Recall number (Z-number) Z-2886-2011
Recall event 58966
Product ***** EXPANDED RECALL ***** Rusch Foley Catheter Insertion Tray with Preconnected Bag and 16 Fr. Catheter, Manufactured for and distributed by Teleflex Medical, Research Triangle Park, NC 57708 Product Usage: For one time use per the Directions for Use with urinary catheter for drainage of urine.
Product code FAQ
Recalling firm Teleflex Medical
Recall class Class II
Status Terminated
Termination date Apr 5, 2013
FEI number 3005747797

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 1–9 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)