Drug recall
Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket, single monitor mount, 27" max. screen size…
FDA recall event 85252 · Class II · Skytron, Div. The KMW Group, Inc
Key facts
| Event ID | 85252 |
|---|---|
| Recall numbers | Z-1569-2020 |
| Recalling firm | Skytron, Div. The KMW Group, Inc |
| Product type | Devices |
| Products | Skytron Ergon 3 Series Skyboom Monitor Bracket-Flatscreen Bracket, single monitor mount, 27" max. screen size Part number 3FCM1 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Potential for the weld to fail at the pivot point of the monitor bracket. This weld failure could cause the display interface and bracket to fall from its mounted location, resulting in injury. |
| Initiation date | Mar 5, 2020 |
| Report date | Apr 1, 2020 |
| City | Grand Rapids |
| State | MI |
| Country | United States |
| FEI number | 1825014 |
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: