Urodiagnost, Product No. 708033 Product Usage: The Philips UroDiagnost MRF can be used to perform all urological and gynecological routine examinations including: Urograms with injection or infusion Retrograde pyelography Cystography and urethrography Micturition cystography Cystoscopy, endopscopy Transurethral resection Percutaneous nephroscopy Urethrorenoscopy Percutaneous nephrolithotomy Serial angiography with image intensifier and DSI Tomography
FDA Recall Z-1053-2019 · Posted None
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Recalling FirmPhilips North America, LLC
Recall StatusTerminated
Product CodeIXR
Date Initiated2019-02-28
Date Terminated2020-08-03
Product Quantity1969
Reason for Recall
The locking plate may be missing from the system, which may result in unexpected stand/table tilt movement that cannot be stopped by the user.
Firm Action
On February 28, 2019, the firm notified customers via an Urgent Field Safety Notice letter. The letter informed customers that the affected systems would be inspected for missing locking plates.
Customers were asked to place a copy of the Field Safety Notice with the documentation of the system until the system has been inspected by Philips.
Philips will inspect all potentially affected systems free of charge. If a locking plate is found missing, Philips will secure the system until a locking plate is installed so that use of the system can continue. You will be contacted by your local Philips representative to schedule the inspection. Philip's action will start effective from March 2019.
If you need further information or support concerning this issue, please contact your local Philips representative.
Root Cause
Component design/selection
Distribution Pattern
US Nationwide domestic distribution, and worldwide international 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.
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