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Philips North America, LLC recalls Urodiagnost, Product No. 708033 Product Usage: The Philips UroDiagnost MRF can be used to perform all urological and
Recalled April 3, 2019 · FDA recall Z-1053-2019 · Philips North America
Hazard
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. · FDA Class II
Units
1969
Sold at
US Nationwide domestic distribution, and worldwide international distribution.
Description
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.
Product
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
Manufacturer(s)
Philips North America, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →