Reported Jun 4, 2025 · Ongoing

Cardiohelp System HKH 8820 Wall Holder. Mounting bracket designed to hold the CARDIOHELP-i system for interhospital…

Maquet Cardiopulmonary Ag

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Maquet Cardiopulmonary Ag · Kehler Str. 31 · Rastatt, N/A · N/A

Is this the product you have?

  • Cardiohelp System HKH 8820 Wall Holder. Mounting bracket designed to hold the CARDIOHELP-i system for interhospital transport by vehicle.
Lot codes and dates
    • Model No. 701045366
    • UDI 04037691456584
    • All Serial No
Amount recalled
US: 2 units; OUS: 168 units

Where it was sold

Why it was recalled

HKH 8820 Wall Holder does not comply with standard DIN EN 1789:20 and has the potential to detach.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:37 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.