FDAOctober 12, 2023device

Cardiohelp-i, blood oxygenation and carbon dioxide removal system, Part Numbers 701072780 (Cardiohelp-i), 701068550 (Slide Rail Holder)

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

The hazard

It was found that the fixation (weld) employed by the supplier of the nut bolt to the slide rail plate was insufficient. The deficient weld allows the nut bolt to break off from the slide rail plate with slight manual force.

What to do

FDA enforcement status: Ongoing

Brands named

maquet medical systemsmaquetmaquet medical

UPCs

04058863074863

Recall history

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

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