Philips Medical Systems DMC GmbH: Device Recall
Recall #Z-0465-2026 · 10/01/2025
Recall Details
- Recall Number
- Z-0465-2026
- 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
- 223 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
DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035;
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
- Class II: Risk 10/01/2025
- Class II: Risk 10/01/2025
- Class II: Risk 10/01/2025
- Class II: Risk 10/01/2025
- Class II: Risk 10/01/2025