FDAJuly 12, 2024device

GE Healthcare Proteus XR/a, stationary X-Ray System, Model/Catalog Numbers: 1) 2259973; 2) 2259988; 3) 2266999; 4) 2373519; 5) 2379827; 6) 5729352; 7) 2259973-1; 8) 2259973-2; 9) 2259973-3; 10) 2259973-4; 11) Not Available

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

The hazard

The XR system, Proteus XR/a, does not have a de-installation manual describing process steps for de-installing the devices. De-installation instruction process steps must be followed when de-installing these devices to avoid personnel injury during de-install.

What to do

FDA enforcement status: Ongoing

Brands named

ge healthcare china

UPCs

008406821207770084068210613983093535827831096051268309437826383089838806830916612418313504876682407110020824070401018240704021682407290043

Recall history

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

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GE Healthcare Proteus XR/a, stationary X-Ray System, Model/Catalog Numbers: 1) 2259973; 2) 2259988; 3) 2266999; 4) 2373519; 5) 2379827; 6) 5729352; 7) 2259973-1; 8) 2259973-2; 9) 2259973-3; 10) 2259973-4; 11) Not Available — Recall Details · AllClear