Integra LifeSciences Corp.: Medical Device Recall in 2017 - (Recall #: Z-1410-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

The UNI-CP System; Model Number: 330230SND.

Product Classification:

Class III

Date Initiated: January 25, 2017

Date Posted: March 15, 2017

Recall Number: Z-1410-2017

Event ID: 76408

Reason for Recall:

The firm received one complaint from one non-US sales representative (France) that the label on the UNI-CP plate was incorrect.

Status: Terminated

Product Quantity: 39 units

Code Information:

Lot # FEDT

Distribution Pattern:

Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated