Customers are directed to call local Philips representative or Philips Customer Service at 1-86.ĥ9 units total (12 units in the US and 47 units outside the US)ĭistributed in the states of CA, IA, KY, MD, NY, PA, UT, VA, WA and WI.Īlso distributed in Australia, Belgium, Canada, India, Italy, Japan, South Korea, Netherlands, New Zealand, Spain, Sweden, and Switzerland.ġ A record in this database is created when a firm initiates a correction or removal action. Philips Medical Systems will also have Customer Reply Cards returned for tracking purposes. 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.
#Philips qlab acmq quick guide software
QLAB Quantification Software is a software application package designed to view and quantify image data acquired on Philips Medical Systems ultrasound products.
#Philips qlab acmq quick guide code
System, image processing, radiological - Product Code LLZ Class 2 Device Recall Philips Ultrasound QLAB
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