Data Foundry

Medical device recalls 2016

Syngo — Class II medical device recall Z-2088-2016

Terminated recall by Siemens Medical Solutions USA, Inc, reported 2016-07-06, distributed in AL, CA, CT, FL, IN, KS, LA, MA…. Software error in previous software versions in which two references for the same image may exist in the datab

Recall numberZ-2088-2016
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmSiemens Medical Solutions USA, Inc, Malvern, PA, United States
Recall initiated2016-05-09
Classified2016-06-29
Reported by FDA2016-07-06
Terminated2017-03-20
DistributedAL, CA, CT, FL, IN, KS, LA, MA, MD, MI, MN, MO, MS, NE, NY, OH, OR, PA, TX, WI
Quantity74 systems
Reason classessoftware
Serial numbers100025, 100027, 100029, 100031, 100033, 100084, 100105, 100106, 100109, 100110, 100111, 100112, 100113, 100114, 100115, 100116, 100117, 100119, 100120, 100132, 100133, 100139, 100140, 100141, 100142 and 47 more
Model numbers10863171, 10863172, 10863173

Product

Syngo.plaza, Picture archiving and communication system (PACS), Model Numbers - 10863171, 10863172, 10863173,

Reason for recall

Software error in previous software versions in which two references for the same image may exist in the database.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2088-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.