Official recall record
Precision CRF; Model Number: 706400;
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2025-10-01
- Country of alert
- Germany
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00884838110588
- Brand on record
- Philips Medical Systems DMC GmbH
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
Other recalls from this brand
- 2025-10-01 · US FDA — Medical Devices
Radiography 7300 C; Model Number: 712037; - 2025-10-01 · US FDA — Medical Devices
DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035; - 2025-10-01 · US FDA — Medical Devices
ProxiDiagnost N90; Model Number: 706110;
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