Philips Medical Systems DMC GmbH: Device Recall

Recall #Z-0466-2026 · 10/01/2025

Class II: Risk

Recall Details

Recall Number
Z-0466-2026
Classification
Class II
Product Type
Device
Recalling Firm
Philips Medical Systems DMC GmbH
Status
Ongoing
Date Initiated
10/01/2025
Location
Hamburg, Germany
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
284 units

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.

Product Description

Radiography 7300 C; Model Number: 712037;

Distribution Pattern

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.,

Other Recalls by Philips Medical Systems DMC GmbH

View all recalls by Philips Medical Systems DMC GmbH →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.