Uroskop Omnia max, Model No. 10762473 - Product Usage: Uroskop Omnia Max is a device intended to visualize anatomical structures by converting an Xray pattern into a visible image. The system is designed primarily for urological diagnosis and the support of urological therapeutic applications such as examinations and small interventions of the urogenital tract.
FDA Recall Z-1333-2020 · Posted None
Advertisement
Recalling FirmSiemens Medical Solutions USA, Inc
Recall StatusTerminated
Product CodeOWB
Date Initiated2020-01-08
Date Terminated2022-06-21
Product Quantity192
Reason for Recall
Siemens became aware of an issue of incorrect use of the bypass key overriding the built-in
collision control creating risk of collision with obstacles or persons when the operator uses the override function.
Firm Action
On January 8, 2020, the firm initiated the recall, notifying customers via Urgent Medical Device Correction letters.
Customers were advised of the potential for a system collision due to incorrect use of the bypass key overriding the built-in collision control. The bypass key is intended to enable movement of an otherwise blocked system to avert immediate hazard, e.g. to recover a patient following device error or in case of emergency. It is not intended for permanent use.
Customers were instructed to use the bypass key exclusively to avert an immediate hazard and immediately contact Siemens Customer Service at 1-800-888-7436 to fix the issue.
Siemens Healthineers will correct the error with a field software update which will be available starting in January 2020, free of charge. Your local Siemens Healthineers Service organization will contact you to arrange a date to perform this corrective action when the software update is available for your system. Customers may contact the firm's service organization for an earlier appointment at 1-800-888-7436.
With this field software update, an additional acoustic signal will be introduced for an event of movement in
an error situation. The signal alerts the user that the system is in the "override" state and special attention
should be paid regarding possible collisions. Following the correction, the cause is eliminated, and any
recurrence of this potential fault is prevented.
Root Cause
Use error
Distribution Pattern
US Nationwide distribution.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
Advertisement