Siemens recalls Uroskop Omnia Max fluoroscopy systems with serial numbers 4032-5078 due to risk of swivel arm dislodging, potentially causing injury during medical imaging procedures.
The swivel arm holding the monitors may become dislodged from the carrying arm.
Siemens is recalling Uroskop Omnia Max fluoroscopic X-ray systems with specific serial numbers because the swivel arm holding monitors could become dislodged from the carrying arm. This poses a risk of injury during medical procedures if the arm becomes detached.
The swivel arm that holds the monitors may become dislodged from the carrying arm during use. If this happens, the monitor could fall or move unexpectedly, potentially causing injury to medical staff or patients during X-ray procedures.
Medical facilities using the recalled Uroskop Omnia Max systems are most at risk. Patients undergoing X-ray procedures with these devices could be affected if the swivel arm becomes dislodged.
Check if your Uroskop Omnia Max fluoroscopy system has a serial number between 4032 and 5078. The device is used for medical imaging to visualize anatomical structures via X-rays.
Verify your device's serial number to see if it falls within the range 4032 to 5078.
Reach out to Siemens Medical Solutions USA, Inc for further instructions on handling the device.
The recalled model is Uroskop Omnia Max with serial numbers ranging from 4032 to 5078.
The swivel arm holding the monitors may become dislodged from the carrying arm, potentially causing injury during medical procedures.
Check if your Uroskop Omnia Max system has a serial number between 4032 and 5078.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-0985-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-0985-2019 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.
