Device recall

Z-2575-2011: Integra Pain Management Disposable, Convenience Kit PICC INSERTION TRAY, Reorder…

FDA device recall · Class I · Integra LifeSciences Corp.

Key facts

Recall number (Z-number) Z-2575-2011
Recall event 58995
Product Integra Pain Management Disposable, Convenience Kit PICC INSERTION TRAY, Reorder Number 3403203, Sterile/EO, Integra LifeSciences Corporation, West Valley City, Utah 84119.
Product code FMF
Recalling firm Integra LifeSciences Corp.
Recall class Class I
Status Terminated
Termination date Aug 1, 2011
510(k) numbers K960248
FEI number 3003418325

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

Browse all FDA device recalls (products)