Drug recall
Integra Disposable, Convenience Kit Single Shot Epidural Tray Reorder Number 340269 Rx Only Product Usage: The…
FDA recall event 66885 · Class II · Integra LifeSciences Corp. d.b.a. Integra Pain Management
Key facts
| Event ID | 66885 |
|---|---|
| Recall numbers | Z-0533-2014 |
| Recalling firm | Integra LifeSciences Corp. d.b.a. Integra Pain Management |
| Product type | Devices |
| Products | Integra Disposable, Convenience Kit Single Shot Epidural Tray Reorder Number 340269 Rx Only Product Usage: The Integra kits which contain a BD LOR syringe are intended to provide licensed medical… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Integra LifeSciences Corporation is recalling certain lots of Integra Kits for Epidural Anesthesia Administration as a result of a Product Advisory Notice from BD Medical for the LOR syringes… |
| Initiation date | Oct 28, 2013 |
| Report date | Dec 25, 2013 |
| Termination date | Jan 29, 2014 |
| 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: