[pending] Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;
Pending LLM rewrite. Source: FDA_DEVICE Z-0719-2026.
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
The motorized longitudinal movement of the FlexArm stand may be inconsistent (not smooth) and eventually may become unavailable. This issue is due to grease leakage from the bearings and/or anti-corrosion oil applied on the bearings, because of which the lubrication on the ceiling rail may be excessive, reducing the friction between the rails and the friction wheel. Expansion to add additional model.
The recalled product
- Product
- Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;
- Manufacturer
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- 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 (1)
- Model Number: 722234
Distribution
Distributed in 28 states:
- AL
- AR
- AZ
- CA
- CO
- FL
- GA
- HI
- IL
- IN
- KS
- KY
- MD
- MN
- MO
- NM
- NY
- OH
- OK
- PA
- RI
- TX
- UT
- VA
- WA
- WI
- WV
- WY
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