FDA Device Recalls

Recalls /

#149423

Product

Syngo.Plaza VB 10 A, image processing system (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images.

FDA product code
LLZSystem, Image Processing, Radiological
Device class
Class 2
Medical specialty
Radiology
510(k) numbers
K132532
Affected lot / code info
Model Numbers: 10863171, 10863172, 10863173, 10592457  Serial Numbers:  100262,100389,100198,100258,100259,100538,100135,100133,100213,100214,100031,100032,100484,100362,100233,100140,100141,100142,100143,100144,100416,100105,100106,100109,100110,100111,100112,100113,100114,100115,100116,100117,100119,100120,100461,100457,100245,100447,100364,100314,100298,100299,100386,200277,100139,100027,100028,100300,100559,100440,100441,100197,100170,100025,100026,100084,100186,100189,100190,100191,100192,100195,100196,100550,100033,100034,100306,100307,100232,100449,100450,100185,100596,100256,100199,100188,100193,100194,100257,100226,100228,100425,100029,100030,100253,100203,100204,100132,100247,100248,100434,100215,100491,100495,100230,100221,100212,100539,100206

Why it was recalled

Siemens is releasing a Customer Advisory Notice to explain meaning of a suffix o.p. that shows on some DICOM images on area, distance or perimeter values. This suffix stands for on projection and indicates that a shown measurement value may be different from the real value.

Root cause (FDA determination)

Error in labeling

Action the firm took

Siemens mailed to customers on August 04, 2016 a Customer Advisory Notice that provided interpretations about the meaning of measurement values like area, distance and perimeter shown as "o.p." by the syngo.plaza.

Recalling firm

Firm
Siemens Medical Solutions USA, Inc
Address
40 Liberty Blvd, Malvern, Pennsylvania 19355-1418

Distribution

Distribution pattern
Nationwide Distribution

Timeline

Recall initiated
2016-08-02
Posted by FDA
2016-09-14
Terminated
2017-03-20
Status

Source: openFDA Device Recall endpoint. Recall record ID #149423. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.