Device recall

Z-1141-03: BiodivYsio SV Over The Wire (OTW) Coronary Stent, 2.25 mm diameter; Catalog #…

FDA device recall · Class II · Abbott Vascular Devices

Key facts

Recall number (Z-number) Z-1141-03
Recall event 26854
Product BiodivYsio SV Over The Wire (OTW) Coronary Stent, 2.25 mm diameter; Catalog #: B3225-10, Lot #: 010586G; Catalog #: B3225-10, Lot #: 030176G; Catalog #: B3225-15, Lot #: 010626G; Catalog #: B3225-18, Lot #: 020246G.
Product code MAF
Recalling firm Abbott Vascular Devices
Recall class Class II
Status Terminated
Termination date Aug 20, 2003
FEI number 3000718335

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 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)