Integra LifeSciences Corp.: Medical Device Recall in 2020 - (Recall #: Z-0725-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Bactiseal Endoscopic Ventricular Catheter: EVC- Catheter is designed for use in the treatment of hydrocephalus when shunting cerebrospinal fluid (CSF) from the ventricles of the brain. Part Number: 823087

Product Classification:

Class II

Date Initiated: December 14, 2020

Date Posted: December 30, 2020

Recall Number: Z-0725-2021

Event ID: 86986

Reason for Recall:

Mislabeled product-Bactiseal Ventricular Catheter with Bactiseal Shunt System(823073) mislabeled as Bactiseal Endoscopic Ventricular Catheter (823087) and vs. versa

Status: Terminated

Product Quantity: 17 units

Code Information:

Lot Number:4178257 Exp. Date: November 2019

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated