Integra LifeSciences Corp. d.b.a. Integra Pain Management: Medical Device Recall in 2016 - (Recall #: Z-2684-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

INTEGRA Spinal Tray, Catalogue No: 3404875, Contents: 10 Each per Case, Sterile.

Product Classification:

Class II

Date Initiated: August 4, 2016

Date Posted: September 7, 2016

Recall Number: Z-2684-2016

Event ID: 74867

Reason for Recall:

Integra LifeSciences is recalling Spinal Trays, Cat No. 3404875, because of the affected recalled Hospira 5% Lidocaine HCL that is a component of some lots of the Spinal Trays.

Status: Terminated

Product Quantity: 200 packages (20 cases)

Code Information:

The affected lots of Integra¿ Spinal Trays were manufactured on 2/11/205 and on 7/11/2015. Lots: W1503004; S1501531; S1505556;

Distribution Pattern:

US Distribution to the states of : OH and CA. No foreign, Govt/VA/military consignee.

Voluntary or Mandated:

Voluntary: Firm initiated