Device recall

Z-0544-2007: Terumo L Series 1863 type arterial perfusion cannulae, straight open tip, 1/4''…

FDA device recall · Class III · Terumo Cardiovascular Systems Corp

Key facts

Recall number (Z-number) Z-0544-2007
Recall event 37104
Product Terumo L Series 1863 type arterial perfusion cannulae, straight open tip, 1/4'' connector, arterial cannula, 12 FR, 17.5 cm (7'') long; Catalog no. L7351.
Product code DWF
Recalling firm Terumo Cardiovascular Systems Corp
Recall class Class III
Status Terminated
Termination date Dec 5, 2007
510(k) numbers K930620
FEI number 1828100

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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