Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Integra Long Epidural Steroid Injection Needle (Tuohy Needle) Recalled by Integra LifeSciences Corp. d.b.a. Integra Pain Management Due to A single lot of 18 Gauge, 3.5 inch...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Integra LifeSciences Corp. d.b.a. Integra Pain Management directly.
Affected Products
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.
Quantity: 90 Tuohy needles (9 cases of 10 each)
Why Was This Recalled?
A single lot of 18 Gauge, 3.5 inch Tuohy Needles were incorrectly packaged and labeled as 18 Gauge, 5 inch needles.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Integra LifeSciences Corp. d.b.a. Integra Pain Management
Integra LifeSciences Corp. d.b.a. Integra Pain Management has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report