Maquet recalls Cardiohelp HKH 882: Wall holder may detach, causing injury. Affected units have model 701045366. Stop using immediately.
HKH 8820 Wall Holder does not comply with standard DIN EN 1789:20 and has the potential to detach.
Maquet is recalling its Cardiohelp HKH 8820 Wall Holder because it may detach from the wall, posing a risk of injury. This recall affects medical devices used for interhospital transport. The hazard requires immediate action to prevent potential injury.
The wall holder does not meet safety standards and can become loose. If it detaches, it may fall and cause injury to people nearby. This is a serious hazard during medical transport operations.
Healthcare professionals using the Cardiohelp HKH 8820 Wall Holder for interhospital transport are most at risk. Patients and staff near the device could be injured if it detaches.
Check for the model number 701045366 on the wall holder. The product was sold with the UDI 04037691456584 and all serial numbers.
Remove the Cardiohelp HKH 8820 Wall Holder from the wall and do not use it until a replacement is obtained.
The wall holder does not comply with safety standards and has the potential to detach, which could cause injury.
Check for model number 701045366 on the wall holder.
The recall record does not mention a fix or remedy.
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-1823-2025 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-1823-2025 from Maquet. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
