Device recall

Z-0590-2008: BD Vacutainer Push Button Blood collection Sets with Pre-Attached Holder…

FDA device recall · Class II · Becton Dickinson & Company

Key facts

Recall number (Z-number) Z-0590-2008
Recall event 45965
Product BD Vacutainer Push Button Blood collection Sets with Pre-Attached Holder; Catalog Number: 368656; 23 g X12 " PBBCS w/PAH (Preattached), BD Diagnostics, Franklin Lakes, NJ
Product code JKA
Recalling firm Becton Dickinson & Company
Recall class Class II
Status Terminated
Termination date Sep 8, 2008
510(k) numbers K011984
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

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