Syngo.via recall: Software Issue
Syngo.via, picture archiving and communications system software controlled. Intended to be used for viewing, manipulation, communication, and storage…
Why was Syngo.via recalled?
Incorrect values for the volume calculation. Software update VB30B via Update Instructions SY018/16/P to resolve software errors.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
310289,130542,130322,310149,130325,221063,310168,101762,221048,221096,220783,310195,130451,400031,130292,310114,220846,130269,130163,130402,130826,221051,102336,310282,220888,10007,221052,221049,130518,221002,221091,220915,130520,130472,100469,310249,130122,100013,130378,310188,102453,310079,310080,130240,130382,220985,310171,220879,220995, and 310268.
- Product
- Syngo.via, picture archiving and communications system software controlled. Intended to be used for viewing, manipulation, communication, and storage…
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 50 units
- Distribution
- Nationwide Distribution -- AR, CA, CO, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, ND, NE, NJ, NM, NV, NY, OH, OK, PA, SC, TX, and UT.
- Recall date
- July 27, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)