Integra LifeSciences Corp.: Medical Device Recall in 2015 - (Recall #: Z-0025-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

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 Classification:

Class II

Date Initiated: August 21, 2015

Date Posted: October 14, 2015

Recall Number: Z-0025-2016

Event ID: 72068

Reason for Recall:

Integra identified that the UCHRAP component (Arc Adapter Plate) would not assemble properly to the UCHRAR component (ARC Adapter Ring) of the Compact Head Ring Adapter due to an error in the manufacturing drawing.

Status: Terminated

Product Quantity: 6 units

Code Information:

Cat. No. UCHRAP; Serial No.s 900, 901, 902, 904, 905, 906

Distribution Pattern:

Worldwide Distribution - US Distribution to the states of : NJ, TX and WY., and to the countries of : Algeria, Germany and India.

Voluntary or Mandated:

Voluntary: Firm initiated