Device recall

Z-2710-2016: BD Vacutainer Push Button Blood Collection Set, Sterile, Rx only, 0.6 x 19 mm x…

FDA device recall · Class II · Becton Dickinson & Company

Key facts

Recall number (Z-number) Z-2710-2016
Recall event 74909
Product BD Vacutainer Push Button Blood Collection Set, Sterile, Rx only, 0.6 x 19 mm x 305 mm, 23G x 3/4" x 12", REF 367342.
Product code JKA
Recalling firm Becton Dickinson & Company
Recall class Class II
Status Terminated
Termination date Nov 20, 2017
510(k) numbers K030573
FEI number 2243072

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 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)