[pending] ProxiDiagnost N90; Model Number: 706110;
Pending LLM rewrite. Source: FDA_DEVICE Z-0461-2026.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Pending LLM scoring against the rubric.
Plain-English summary
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.
The recalled product
- Product
- ProxiDiagnost N90; Model Number: 706110;
- Manufacturer
- Philips Medical Systems DMC GmbH
- Category
- Medical Device — Devices
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.
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