The Recall Desk
Agency classClass IIOur severity:ModerateFDA (Devices)·Z-0463-2026·Announced 2025-11-19

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.

The agency’s classification

FDA (Devices): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 2/5 (Moderate).

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
Category
Medical Device — Radiography system
Hazard
Affected units
42

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.

Part of a larger recall action

This product is one of 6 recalled by Philips Medical Systems DMC GmbH under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 6 products in this recall →

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