The Recall Desk
Agency classClass IIOur severity:ModerateFDA (Devices)·Z-0461-2026·Announced 2025-11-19

ProxiDiagnost systems recalled over ceiling carriages that resist vertical movement

Philips is recalling 41 ProxiDiagnost N90 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 ProxiDiagnost N90, model 706110, 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 41 units carrying UDI-DI 00884838103221, 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
ProxiDiagnost N90; Model Number: 706110;
Manufacturer
Philips Medical Systems DMC GmbH
Category
Medical Device — Radiography system
Hazard
Affected units
41

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: 706110
  • UDI-DI: 00884838103221
  • Serial Number: 10001185
  • 10001205
  • 10001220
  • 10001224
  • 10001225
  • 10001227
  • 10001228
  • 10001229
  • 10001230
  • 10001231
  • 10001234
  • 10001235
  • 10001236
  • 10001237
  • 10001239
  • 10001245
  • 10001247
  • 10001248

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 →

Related recalls

Same manufacturer · Philips Medical Systems DMC GmbH

See all →

Same hazard · manufacturing defect

See all →

Similar recalls