Siemens recalls Uroskop Omnia Max X-ray systems with serial numbers starting 4036-5222 due to potential support arm dislodgement after prolonged intense use.
After the March 2019 corrective action on the monitor support arm, there is a residual risk of the support arm becoming dislodged in cases when the monitor support arm is used intensely over a long period of time.
Siemens is recalling Uroskop Omnia Max X-ray systems with specific serial numbers because the monitor support arm could become dislodged after long periods of heavy use. This poses a risk of the arm becoming loose and potentially causing injury during medical procedures.
After a March 2019 fix, the support arm can still become dislodged if used intensely over long periods. This could lead to the arm moving unexpectedly during medical procedures, potentially causing injury to the patient or operator.
Healthcare professionals using the Uroskop Omnia Max X-ray system for urological procedures are most at risk. Patients undergoing these procedures may also be affected if the system malfunctions.
Check for serial numbers starting with 4036 to 5222 on the Uroskop Omnia Max X-ray system. This model is used for urological procedures like endourology and minimal invasive surgery.
Inspect the monitor support arm for signs of looseness or movement after prolonged use. If it feels unstable, stop using the system immediately.
After a March 2019 corrective action, there is a residual risk of the support arm becoming dislodged when used intensely over long periods.
Check the serial number on your Uroskop Omnia Max X-ray system. If it starts with 4036-5222, inspect the support arm for looseness. If unstable, stop using it immediately.
The recall does not mention a specific fix. Users should monitor the support arm for instability and stop using it if it becomes loose.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-0806-2021 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-0806-2021 from Siemens. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
