FDAApril 30, 2025device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Ongoing

Brands named

maquet cardiopulmonary agmaquetmaquet cardiopulmonary

UPCs

04037691456584

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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