Drug recall
Product Name: GCX Channel Mounting Accessory Model/Catalog Number: H8-300-40-A
FDA recall event 90400 · Class II · Skytron, Div. The KMW Group, Inc
Key facts
| Event ID | 90400 |
|---|---|
| Recall numbers | Z-1309-2022 |
| Recalling firm | Skytron, Div. The KMW Group, Inc |
| Product type | Devices |
| Products | Product Name: GCX Channel Mounting Accessory Model/Catalog Number: H8-300-40-A |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Under certain circumstances, the mounting screws may loosen or pull out from the attachment point on the Ergon 3 boom when the GCX Channel Mounting Accessory was used with the VST clamp as a monitor… |
| Initiation date | Jun 2, 2022 |
| Report date | Jul 6, 2022 |
| 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: