# FDA recall Z-0465-2026

> **Philips Medical Systems DMC GmbH** · Class II · device recall initiated 2025-10-01.

## Product

DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER;  Model Number: (1) 712034, (2) 712035;

## 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.

## 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.,

## Key facts

- **Recall number:** Z-0465-2026
- **Recalling firm:** Philips Medical Systems DMC GmbH
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-10-01
- **Report date:** 2025-11-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Hamburg, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0465-2026

## Citation

> AI Analytics. FDA recall Z-0465-2026. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/Z-0465-2026. Source: US FDA. Licensed CC0.

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