Precision CRF systems recalled over ceiling carriages that are hard to move
Philips is recalling 42 Precision CRF systems because some ceiling suspension telescopic carriages may be difficult to move vertically.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: Scored 2 because the record describes extra force needed to move a component, without stating a health consequence or reported harm.
Plain-English summary
The Philips Precision CRF, model 706400, is being recalled.
Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically, requiring additional force or physical exertion for manual movement, due to potential manufacturing issues.
The recall covers 42 units carrying UDI-DI 00884838110588, distributed worldwide including nationwide in the United States and to countries including Australia and Austria. The FDA has classified the action as Class II.
The enforcement record describes the additional force required without stating a health consequence, and reports no injuries. Sites operating an affected system should follow Philips' instructions.
The recalled product
- Product
- Precision CRF; Model Number: 706400;
- Manufacturer
- Philips Medical Systems DMC GmbH
- Hazard
- manufacturing-defect
- restricted-movement
- ceiling-suspension
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- Model Number: 706400
- UDI-DI: 00884838110588
- Serial Number: 19
- 28
- 29
- 30
- 31
- 32
- 33
- 34
- 35
- 36
- 37
- 38
- 39
- 40
- 10001178
- 10001179
- 10001181
- 10001182
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- SevereABIOMED Introducer Kit 23 Fr heart pump accessory leakage risk
FDA (Devices) · 2026-07-22
- HighGE Medical Optima XR200/220/240amx Mobile Radiographic Systems Recall
FDA (Devices) · 2026-07-22
- SevereABIOMED Impella RP Flex heart pump introducer sheath leakage risk
FDA (Devices) · 2026-07-22
- ModeratePapablic Replacement Brush Heads Recalled for Potential Breakage
FDA (Devices) · 2026-07-22
- HighRapid Refill Continuous Injection System Recalled for Syringe Loosening Risk
FDA (Devices) · 2026-07-22