CanadaCertain Philips Diagnostic X‑Ray Systems — CombiDiagnost R90 (model 709031), Digital Diagnost (models 9890 010 8390X and 9890 010 83904), Radiography 7300 C (model 712037), and DigitalDiagnost C90 (model 9890 010 83905) — with ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be identified by those model/catalogue numbers. They were recalled because the telescopic carriages may be difficult to move vertically, requiring additional force due to potential manufacturing issues; contact the manufacturer for additional information.
What's being recalled
Companies: Philips Medical Systems Nederland B.V., Veenpluis 6, Best, Netherlands, 5684 PC.
How to identify it
Affected products: CombiDiagnost R90; Lot or serial number: Not applicable.; Model or catalogue number: 709031
Affected products: Digital Diagnost; Lot or serial number: Not applicable.; Model or catalogue number: 9890 010 8390X
Affected products: Digital Diagnost; Lot or serial number: Not applicable.; Model or catalogue number: 9890 010 83904
Affected products: Radiography 7300 C; Lot or serial number: Not applicable.; Model or catalogue number: 712037
Affected products: DigitalDiagnost C90; Lot or serial number: Not applicable.; Model or catalogue number: 9890 010 83905
The hazard
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
Contact the manufacturer if you require additional information.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)