PlainRecalls
FDA Devices Moderate Class II Ongoing

Radiography 7300 C; Model Number: 712037;

Reported: November 19, 2025 Initiated: October 1, 2025 #Z-0466-2026

Product Description

Radiography 7300 C; Model Number: 712037;

Reason for Recall

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.

Details

Units Affected
284 units
Distribution
Worldwide Distribution: US (Nationwide) Distribution and OUS (International) countries of: Australia, Austria, Bahrain, Belgium, Bosnia-Herz., Canada, Chile, Croatia, Denmark, Estonia, Finland, France, Germany, Ghana, Gibraltar, Guadeloupe, Indonesia, Iraq, Israel, Italy, Jordan, Kuwait, Kyrgyzstan, Latvia, Lithuania, Netherlands, New Zealand, Norway, Panama, Philippines, Poland, Portugal, R¿union, Samoa, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sweden, Switzerland, T¿rkiye, Turkmenistan, United Kingdom, Utd.Arab.Emir.,
Location
Hamburg

Frequently Asked Questions

What product was recalled?
Radiography 7300 C; Model Number: 712037;. Recalled by Philips Medical Systems DMC GmbH. Units affected: 284 units.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 19, 2025. Severity: Moderate. Recall number: Z-0466-2026.