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Philips representatives will distribute the letter internationally.įollow-up letters to wholesale customers will be provided and wholesalers are requested to forward copies of recall letters and response forms to their customers. Philips Medical Systems notified customers of the voluntary recall by sending a certified URGENT-Medical Device Correction letter, dated 2014 JUL 09, to all US and Canadian consignees. The QLAB a2DQ and aCMQ features have a defect that may use incorrect measurement values under specific conditions.
Qlab philips serial numbers#
There are licensing agreements with these distributors that allows the distributors to create their own licensing and serial numbers and/or tracking information. ***********Two units shipped in US and one unit shipped outside the US to distributors do not have serial numbers.
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QLAB Quantification Software is a software application package designed to view and quantify image data acquired on Philips Medical Systems ultrasound products. System, image processing, radiological - Product Code LLZ Class 2 Device Recall Philips Ultrasound QLAB