Device recall

Z-0025-2016: Universal Compact Head Ring Adapter Plate (UCHRAP), a component of the Universal…

FDA device recall · Class II · Integra LifeSciences Corp.

Key facts

Recall number (Z-number) Z-0025-2016
Recall event 72068
Product Universal Compact Head Ring Adapter Plate (UCHRAP), a component of the Universal Compact Head Ring Adapter, UCHRA. The UCHRA is a component of the Integra CRW Precision Arc Stereotactic System.
Product code HAW
Recalling firm Integra LifeSciences Corp.
Recall class Class II
Status Terminated
Termination date Oct 13, 2016
510(k) numbers K944463
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

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