Recall events
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Event 83415
Event summary
Timeline bucket July 09, 2019
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
4 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 4
MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914
Z-2342-2019
Recall number Z-2342-2019
Initiated July 09, 2019
Classification Class II
Status Terminated
Quantity 143
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2342-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44610]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
Code information Serial # 41878 52409 142129 141526 42163 152267 141686 42436 42160 142132 41953 141226 141862 141521 42225 52171 41980 41051 152232 42247 141462 52299 52338 42416 141199 141557 142109 141054 152249 42020 41794 142147 152217 141951 42458 141638 42087 142010 42326 142009 142124 141676 42290 52229 42298 142130 141561 141973 42530 141141 41951 42236 152215 42267 42364 141305 42372 142122 42083 142142 42217 52195 152175 41945 141712 42256 42310 41780 42422 141963 42534 52350 52249 42412 42413 52397 41862 141786 42420 52221 52304 42306 141513 142024 141016 42495 142120 41906 52267 141589 42249 42158 41897 52321 42303 141056 42353 42330 41778 141275 141109 142107 42381 42339 41777 152234 52190 141201 42566 141677 41782 42254 42214 52192 141314 141585 42248 42295 42517 141072 42417 141439 141975 142104 41941 41813 141260 42533 141386 52157 141154 141135 142128 141121 142077 141242 142074 141253 141043 141221 42635 42507 141025
Distribution pattern AL AR AZ CA CO CT DC DE FL GA GU IA ID IL IN KS KY LA MA MD ME MI MN MO MT NC NE NH NJ NY OH OK OR PA SC TN TX VA WA WI WV WY
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[28741]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 4
MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915
Z-2343-2019
Recall number Z-2343-2019
Initiated July 09, 2019
Classification Class II
Status Terminated
Quantity 44
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2343-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[10706]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
Code information Serial # 46066 45732 46182 45735 45805 46171 45693 45886 45988 45881 46144 46044 46176 46179 46032 46238 145161 46127 45774 45968 46196 46175 45681 46007 46021 46105 46142 45928 45815 46150 145302 45878 46239 46026 145403 45667 145536 45970 45839 45982 46145 46298 45777 46294
Distribution pattern AL AR AZ CA CO CT DC DE FL GA GU IA ID IL IN KS KY LA MA MD ME MI MN MO MT NC NE NH NJ NY OH OK OR PA SC TN TX VA WA WI WV WY
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[28825]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 4
MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643
Z-2344-2019
Recall number Z-2344-2019
Initiated July 09, 2019
Classification Class II
Status Terminated
Quantity 2
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2344-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32859]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
Code information Serial # 72030 72023
Distribution pattern AL AR AZ CA CO CT DC DE FL GA GU IA ID IL IN KS KY LA MA MD ME MI MN MO MT NC NE NH NJ NY OH OK OR PA SC TN TX VA WA WI WV WY
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[29100]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 4
MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582
Z-2345-2019
Recall number Z-2345-2019
Initiated July 09, 2019
Classification Class II
Status Terminated
Quantity 17
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Device Design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-2345-2019
Source locator 0001-device-recall-0001-of-0001.json.zip#results[32854]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
Code information Serial # 66109 66111 166049 66047 166037 66102 66027 66053 66094 66028 66069 66092 66046 66082 166097 66044 166082
Distribution pattern AL AR AZ CA CO CT DC DE FL GA GU IA ID IL IN KS KY LA MA MD ME MI MN MO MT NC NE NH NJ NY OH OK OR PA SC TN TX VA WA WI WV WY
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[29643]
FDA event record
· Exact recall-number query on openFDA
