Drug recall
Synthes VA Implant Rack for the Compact Distal Radius System Tray/Surgical/Instrument
FDA recall event 75828 · Class II · Synthes (USA) Products LLC
Key facts
| Event ID | 75828 |
|---|---|
| Recall numbers | Z-0867-2017 |
| Recalling firm | Synthes (USA) Products LLC |
| Product type | Devices |
| Products | Synthes VA Implant Rack for the Compact Distal Radius System Tray/Surgical/Instrument |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The screw rack plate was assembled incorrectly which could cause the screws in the screw rack to sit low and touch the surface beneath the screw rack. |
| Initiation date | Nov 29, 2016 |
| Report date | Dec 28, 2016 |
| Termination date | Aug 3, 2017 |
| City | West Chester |
| State | PA |
| Country | United States |
| FEI number | 3008812560 |
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: