Device recall

Z-0212-2008: Thoratec Implantable Ventricular Assist Device (IVAD pump) (Component of…

FDA device recall · Class I · Thoratec Corp

Key facts

Recall number (Z-number) Z-0212-2008
Recall event 45486
Product Thoratec Implantable Ventricular Assist Device (IVAD pump) (Component of Thoratec Ventricular Assist Device (VAD) System), Catalog No. 10012-2555-001 ,Thoratec Corporation, Pleasanton, CA. 94588
Product code DSQ
Recalling firm Thoratec Corp
Recall class Class I
Status Terminated
Termination date May 26, 2009
PMA numbers P870072, P870072S027
FEI number 2916596

At a glance

  • None 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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