Drug recall
INTEGRA Spinal Tray, Catalogue No: 3404875, Contents: 10 Each per Case, Sterile.
FDA recall event 74867 · Class II · Integra LifeSciences Corp. d.b.a. Integra Pain Management
Key facts
| Event ID | 74867 |
|---|---|
| Recall numbers | Z-2684-2016 |
| Recalling firm | Integra LifeSciences Corp. d.b.a. Integra Pain Management |
| Product type | Devices |
| Products | INTEGRA Spinal Tray, Catalogue No: 3404875, Contents: 10 Each per Case, Sterile. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Aug 4, 2016 |
| Report date | Sep 7, 2016 |
| Termination date | Dec 19, 2016 |
| City | Salt Lake City |
| State | UT |
| Country | United States |
| FEI number | 1000138491 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: