Device recall

Z-1480-2021: Tubing with male luer lock adapter (Component) a. 76 cm, REF 601280 b. 122 cm…

FDA device recall · Class II · Smiths Medical ASD Inc.

Key facts

Recall number (Z-number) Z-1480-2021
Recall event 87647
Product Tubing with male luer lock adapter (Component) a. 76 cm, REF 601280 b. 122 cm, REF 607281. component of extravascular blood-pressure Transducer.
Product code DRS
Recalling firm Smiths Medical ASD Inc.
Recall class Class II
Status Terminated
Termination date Mar 20, 2023
FEI number 3012307300

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)