Integra LifeSciences Corp. d.b.a. Integra Pain Management: Medical Device Recall in 2015 - (Recall #: Z-1544-2015)

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:

Integra Long Epidural Steroid Injection Needle (Tuohy Needle), 18 Gauge x 5 inch Removable Wing, Metal Stylet, Calibrations (10BX), Catalogue No. PITRW1850. Used to administer steroid medication in the epidural space.

Product Classification:

Class II

Date Initiated: March 30, 2015

Date Posted: May 6, 2015

Recall Number: Z-1544-2015

Event ID: 70873

Reason for Recall:

A single lot of 18 Gauge, 3.5 inch Tuohy Needles were incorrectly packaged and labeled as 18 Gauge, 5 inch needles.

Status: Terminated

Product Quantity: 90 Tuohy needles (9 cases of 10 each)

Code Information:

Lot No. W1412086, Exp DEC-2017.

Distribution Pattern:

Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated