CombiDiagnost R90; Model Number: 709031;
Reported: November 19, 2025 Initiated: October 1, 2025 #Z-0462-2026
Product Description
CombiDiagnost R90; Model Number: 709031;
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
- Recalling Firm
- Philips Medical Systems DMC GmbH
- Units Affected
- 17 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? ▼
CombiDiagnost R90; Model Number: 709031;. Recalled by Philips Medical Systems DMC GmbH. Units affected: 17 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-0462-2026.
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