Drug recall
Stryker Reliance AL Implant Blocker (Various sizes) The SLIDE Implant Blocker is a reusable instrument…
FDA recall event 62415 · Class II · Stryker Spine
Key facts
| Event ID | 62415 |
|---|---|
| Recall numbers | Z-2176-2012 |
| Recalling firm | Stryker Spine |
| Product type | Devices |
| Products | Stryker Reliance AL Implant Blocker (Various sizes) The SLIDE Implant Blocker is a reusable instrument, sterilized prior to use. It allows the surgeon to distract the disc space in the lumbar region… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Stryker Spine has received six reports regarding the breakage of one or more prongs at the extremity of the instrument. |
| Initiation date | Mar 21, 2011 |
| Report date | Aug 15, 2012 |
| Termination date | Mar 21, 2013 |
| City | Allendale |
| State | NJ |
| Country | United States |
| FEI number | 3004024955 |
At a glance
- 1–9 Products in this recall
- 10–99 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: