Integra LifeSciences Corp.: Medical Device Recall in 2020 - (Recall #: Z-0724-2021)

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 Ventricular Catheter with Bactiseal Shunt System - Product Usage: use in the treatment of hydrocephalus as a component of a shunt system when draining or shunting cerebrospinal fluid (CSF) Part Number: 823073

Product Classification:

Class II

Date Initiated: December 14, 2020

Date Posted: December 30, 2020

Recall Number: Z-0724-2021

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: 85 units

Code Information:

Lot Number: 4178253 Exp. Date: November 2019

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated