Recall events
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Event 75171
Event summary
Timeline bucket September 06, 2016
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording Siemens Medical Solutions USA, Inc
Dossier provenance
Source snapshots represented here
openFDA Device Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall
event_date_initiated coverage
June 01, 1997–June 30, 2026
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Complete imported group
Every recalled product in this event
2 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
device · product 1 of 2
Syngo.plaza, Picture Archiving and Communication System
Z-2891-2016
Recall number Z-2891-2016
Initiated September 06, 2016
Classification Class II
Status Terminated
Quantity 47 systems
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Software upgrade to eliminate several issues
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2891-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[56784]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Software upgrade to eliminate several issues
Code information Serial Numbers: 100262 100198 100258 100259 100538 100133 100213 100214 100031 100484 100362 100416 100461 100457 100447 100139 100027 100559 100440 100441 100025 100084 100186 100189 100190 100191 100192 100195 100196 100033 100232 100449 100450 100199 100256 100228 100425 100029 100253 100203 100204 100132 100434 100491 100495 100206
Distribution pattern Distributed Nationwide
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[23109]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 2
Syngo.plaza VB10A, Picture Archiving and Communication System
Z-2892-2016
Recall number Z-2892-2016
Initiated September 06, 2016
Classification Class II
Status Terminated
Quantity 47 systems
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Software upgrade to eliminate several issues
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Software design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2892-2016
Source locator 0001-device-recall-0001-of-0001.json.zip#results[27153]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Software upgrade to eliminate several issues
Code information Serial Numbers: 100262 100198 100258 100259 100538 100133 100213 100214 100031 100484 100362 100416 100461 100457 100447 100139 100027 100559 100440 100441 100025 100084 100186 100189 100190 100191 100192 100195 100196 100033 100232 100449 100450 100199 100256 100228 100425 100029 100253 100203 100204 100132 100434 100491 100495 100206
Distribution pattern Distributed Nationwide
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[25466]
FDA event record
· Exact recall-number query on openFDA
