Device recall

Z-0494-2019: KIT URIN CUP 16X100 8.0 CONI UA YEL, Cat. No. 364989 BD Vacutainer Urine Cup Kit…

FDA device recall · Class II · Becton Dickinson & Company

Key facts

Recall number (Z-number) Z-0494-2019
Recall event 81148
Product KIT URIN CUP 16X100 8.0 CONI UA YEL, Cat. No. 364989 BD Vacutainer Urine Cup Kit with UA Tube for Midstream Specimens
Product code JTW
Recalling firm Becton Dickinson & Company
Recall class Class II
Status Terminated
Termination date Oct 21, 2020
FEI number 2243072

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)