[Recalled] INTEGRA Spinal Tray, Catalogue No: 3404875, Contents: 10 Each per Case, Sterile. — Integra LifeSciences is recalling Spinal Trays, Cat No | FDA 2016-08-04
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | INTEGRA Spinal Tray, Catalogue No: 3404875, Contents: 10 Each per Case, Sterile. |
|---|---|
| Brand / manufacturer | Integra LifeSciences Corp. d.b.a. Integra Pain Management |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2684-2016 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 04 August 2016 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Integra LifeSciences Corp. d.b.a. Integra Pain Management
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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