Drug recall
Cardiohelp System HKH 8820 Wall Holder. Mounting bracket designed to hold the CARDIOHELP-i system for…
FDA recall event 96820 · Class II · Maquet Cardiopulmonary Ag
Key facts
| Event ID | 96820 |
|---|---|
| Recall numbers | Z-1823-2025 |
| Recalling firm | Maquet Cardiopulmonary Ag |
| Product type | Devices |
| Products | Cardiohelp System HKH 8820 Wall Holder. Mounting bracket designed to hold the CARDIOHELP-i system for interhospital transport by vehicle. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | HKH 8820 Wall Holder does not comply with standard DIN EN 1789:20 and has the potential to detach. |
| Initiation date | Apr 30, 2025 |
| Report date | Jun 4, 2025 |
| City | Rastatt |
| Country | Germany |
| FEI number | 3009507273 |
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: