Medical device recalls Moderate risk

Integra LifeSciences Corp. d.b.a. Integra Pain Management recalls INTEGRA Spinal Tray, Catalogue No: 3404875, Contents: 10 Each per Case, Sterile.

Recall date
August 4, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2684-2016
FDA classification
Class II
Brand / firm
Integra LifeSciences Corp. d.b.a. Integra Pain Management
Sold / distributed
US Distribution to the states of : OH and CA. No foreign, Govt/VA/military consignee.

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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

Get recall alerts

Free email alert whenever Integra LifeSciences Corp. d.b.a. Integra Pain Management has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Integra LifeSciences Corp. d.b.a. Integra Pain Management