FDA Device Intelligence
HomeDRGEM Corporation › DRGEM

DRGEM

DRGEM Corporation · Model GXR-32S · UDI-DI 08800011120146

KPR Prescription
10
510(k) clearances
1,218
Adverse events (5 deaths)
168
Recalls
82
Facilities

Description

480V3~ / 125kV

Recalls

DateFirmReason
2026-01-09FUJIFILM Healthcare Americas CorporationIt was found that the contacts of the electromagnetic contactors used inside the cabinet of the X-ray high-voltage generator were welded, and the current might continue to be suppl
2025-10-01Philips Medical Systems DMC GmbHPhilips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/ph
2025-10-01Philips Medical Systems DMC GmbHPhilips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/ph
2025-09-15FUJIFILM Healthcare Americas CorporationIt was found that the shaft for mounting the X-ray tube unit on the support may break. In addition, it was found that the protective parts might not work effectively only when the
2025-03-10Philips North America LlcPotential for collimator to fall as a result of incorrect installation.
2025-03-10Philips North America LlcPotential for collimator to fall as a result of incorrect installation.
2025-01-28GE Medical Systems, LLCThe user can continue to take the next exposure after reaching the Automatic Exposure Control (AEC) limit, without taking any further actions to acknowledge or adjust exposure tech
2025-01-28GE Medical Systems, LLCThe user can continue to take the next exposure after reaching the Automatic Exposure Control (AEC) limit, without taking any further actions to acknowledge or adjust exposure tech
2025-01-28GE Medical Systems, LLCThe user can continue to take the next exposure after reaching the Automatic Exposure Control (AEC) limit, without taking any further actions to acknowledge or adjust exposure tech
2025-01-28GE Medical Systems, LLCThe user can continue to take the next exposure after reaching the Automatic Exposure Control (AEC) limit, without taking any further actions to acknowledge or adjust exposure tech

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.