Official recall record

DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035;

What the authority reported

Philips 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/physical exertion required for manual movement) due to potential manufacturing issues.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

More recalls: US FDA — Medical Devices · Germany · all filters

Same barcode in other registries

The same EAN appears in 1 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.

• 2023-09-21 · US FDA — Medical Devices
  DigitalDiagnost C90 High Performance, used to acquire, process, store, display and export digital radiographic images.

Other recalls from this brand

• 2025-10-01 · US FDA — Medical Devices
  Radiography 7300 C; Model Number: 712037;
• 2025-10-01 · US FDA — Medical Devices
  Precision CRF; Model Number: 706400;
• 2025-10-01 · US FDA — Medical Devices
  ProxiDiagnost N90; Model Number: 706110;