Drug recall
RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U
FDA recall event 75485 · Class III · Stryker Instruments Div. of Stryker Corporation
Key facts
| Event ID | 75485 |
|---|---|
| Recall numbers | Z-0584-2017 |
| Recalling firm | Stryker Instruments Div. of Stryker Corporation |
| Product type | Devices |
| Products | RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Stryker Instruments is voluntarily recalling the Care Instructions/Instructions for Use packaged with the Radiofrequency (RF) MultiGen¿ Generator, because the instructions for use incorrectly… |
| Initiation date | Oct 11, 2016 |
| Report date | Nov 23, 2016 |
| Termination date | Jul 25, 2017 |
| City | Portage |
| State | MI |
| Country | United States |
| FEI number | 1811755 |
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: