Recall events
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Event 79665
Event summary
Timeline bucket February 01, 2018
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
7 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 7
SOMATOM Emotion 6 (Model 10165888)
Z-2472-2018
Recall number Z-2472-2018
Initiated February 01, 2018
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
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-2472-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[38619]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall A potential risk of unnecessary radiation exposure due to a software issue
Code information Serial No. 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888 10165888
Distribution pattern 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[26896]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 7
SOMATOM Emotion 16 (10165977)
Z-2473-2018
Recall number Z-2473-2018
Initiated February 01, 2018
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
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-2473-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[56380]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall A potential risk of unnecessary radiation exposure due to a software issue
Code information Serial No. 32515 85907 32310 80551 32254 32156 32109 32319 80857 80640 80981 85661 85575 86359 32322 80849 32567 80413 86757 32370 32448 86521 32317 32504 86522 32568 80811 32190 85980 32490 32477 80525 80584 32552 80411 32587 86060 32526 85584 32185 32563 32364 32415 85765 32187 85756 85757 85657 32514 85913 80410 32295 32473 80988 86089 32120 80461 86405 32408 32512 32118 32309 32378 80475 32478 80531 32420 80755 85794 80876 80826 32123 32139 80836 80916 32159 80586 80862 80595 85875 32537 32472 80523 80519 80874 32401 80840 86286 86844 32605 32237 32674 32198 32673 80441 85520 80405 80762 85865 85641 85562 86431 86662 80795 85929 85543 32628 86022 32594 86368 85862 32461 85861 86401 80656 32326 80516 80873 32259 86360 86425 80706 80442 86429 32503 85656 86057 32334 80605 32407 32323 32124 32117 32229 32257 32375 32406 86284 32212 85960 86007 85852 85987 85999 32371 80444 86557 32298 85596 32315 32441 85653 32363 86013 32529 32532 32268 80548 32643 80976 80832 32200 32225 32244 85692 32221 32596 32252 32357 85538 80831 86320 32417 32452 32125 86032 32180 32126 32293 32227 32349 32641 32495 32427 32216 32581 80700 80498 85687 32573 85595 86605 80902 32591 80671 80467 86243 80600 80750 86714 80466 80518 80505 80530 32412 86208 80599 80937 86632 32637 32301 80973 32339 80479 32597 80430 32624 80815 86142 86292 86128 85842 86514 80927 32141 32277 32226 32424 32425 80659 32411 32391 32292 32127 86515 80637 80629 32281 32129 32492 32273 32469 85914 85795 32551 32213 80446 86287 32470 32320 85693 32402 80672 32324 32578 32531 32610 32488 32368 80485 80871 32215 32409 32376 80797 86357 80594 80474 32435 32432 86052 86285 80683 32346 80535 32270 80677 32493 32303 32580 80591 32328 32362 80823 32395 86358 32447 32169 80696 80526 80628 32589 32442
Distribution pattern 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[27664]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 7
SOMATOM Perspective (Model 10495568)
Z-2474-2018
Recall number Z-2474-2018
Initiated February 01, 2018
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
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-2474-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[56383]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall A potential risk of unnecessary radiation exposure due to a software issue
Code information Serial No. 59298 59019 59195 59686 59060 59045 59050 59223 59038 59024 59052 59182 59041 59251 77649 120960 59163 59056 59339 59342 59352 59380 77111 59283 59295 59302 59314 59717 59310 59017 77457 59197 77480 59677 77679 77453 77466 59313 59278 59400 59023 59166 59702 59043 59383 120977 59317 59164 121003 59657 59018 59221 59034 77432 59353 59267 59237 59029 59681 59330 59359 59189 59051 59042 59389 77130 77591 77560 59344 59204 59350 59343 77578 59049 121004 59288 77523 77557 59218 59225 77403 77411 59207 77532 59268 77549 77428 59320 59293 76954 59021 59324 59362 59708 59354 120987 59663 59228 59010 59200 59653 59672 59222 59206 59710 59391 59376 59242 59358 59031 59355 59674 59390 59690 59185 59346 59048 59258 59703 59260 59719 59671 59334 59323 59169 59374 77410 59246 59284 77107 77110 77581 59011 59030 59369 59224 59290 59312 76953 59171 59304 59289 77465 76973 77460 59249 77598 77119 59255 59393 76939 59377 59259 120978 59240 59168 120963 59167 59365 59658 59216 120982 59713 59716 59704 59654 77525 59013 77387 59162 59190 59366 59348 59692 59047 59230 77308 59394 59025 59061 59064 77121 77123 59378 59172 59699 77521 59285 59274 59318 77573 77506 59301 59287 59282 59676 77516 77527 77541 77675 59698 76944 59006 59008 59028 77489 59231 59711 59335 59662 59382 59336 59696 59714 77440 76933 59349 59385 59248 59065 59205 59700 59341 77493 59328 59668 59257 59239 59236 59303 59165 77488 59209 59351 59679 59020 59275 77672 77599 59281 59181 59361 59399 77397 59233 59238 59243 59037 59261 59685 59300 59707 59188 59036 59327 59022 59040 59256 59381 121007 77444 77454 59666 59252 59035 59709 59254 59005 59183 59277 59016 59684 59396 59363 59397 59046 59372 59694 59667 59215 59286 59291 59053 76936 59271 59660 120950 59305 77101 77322 77357 77392 77531 59027 59032 59220 77595 59715 59184 59387 59270 59273 59280 77602 59279 59689 76950 59321 59340 59203 59661 59316 59229 59272 59214 59245 59364 59683 59235 77621 59682 59326 59331 77623 59059 59311 59292 59219 59306 59266 59015 59315 59299 59388 77565 59265 59325 59375 59695 59194 59161 59395 59202 59333 59226 59373 59345 59054 59062 59338 59691 59264 59063 59227 59392 77169 77182 59250
Distribution pattern 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[26684]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 7
SOMATOM Perspective 16 (Model 10891666)
Z-2475-2018
Recall number Z-2475-2018
Initiated February 01, 2018
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
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-2475-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[45959]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall A potential risk of unnecessary radiation exposure due to a software issue
Code information Serial No. 87559 87579 87532 87539 87563 87565 87560 87555 87556 87553 87554 87526 87567 87561 87589 87569 87535 87525 87548 87541 87558 87533 87537 87522 87542 87534 87549 87546 87584 87574 87552 87600 87577 87571 87528 87540 87594 87544
Distribution pattern 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[26920]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 7
SOMATOM Scope ( Model 10967666)
Z-2476-2018
Recall number Z-2476-2018
Initiated February 01, 2018
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
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-2476-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[34140]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall A potential risk of unnecessary radiation exposure due to a software issue
Code information Serial No. 99329 98809 98886 99041 91203 91342 91475 98908 99019 99199 99248 99278 91286 98840 90872 90811 91486 98925 99049 91176 90939 91417 99258 91206 99296 91201 99295 99004 98991 90916 91090 99305 99179 91213 91402 91196 99244 90942 91133 91393 91506 99110 91494 91132 91204 98807 98875 99015 91418 91474 91108 91178 98926 91057 91179 91360 91367 99150 91310 91473 91396 99111 91263 91543 91190 91191 90907 91265 91416 99127 99255 99018 91355 91419 98814 91369 91222 91291 99274 99005 91376 91081 98855 91264 98788 90906 91325 91256 91038
Distribution pattern 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[26940]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 7
SOMATOM Scope Power (Model 10967888)
Z-2477-2018
Recall number Z-2477-2018
Initiated February 01, 2018
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
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-2477-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[34138]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall A potential risk of unnecessary radiation exposure due to a software issue
Code information Serial No. 99329 98809 98886 99041 91203 91342 91475 98908 99019 99199 99248 99278 91286 98840 90872 90811 91486 98925 99049 91176 90939 91417 99258 91206 99296 91201 99295 99004 98991 90916 91090 99305 99179 91213 91402 91196 99244 90942 91133 91393 91506 99110 91494 91132 91204 98807 98875 99015 91418 91474 91108 91178 98926 91057 91179 91360 91367 99150 91310 91473 91396 99111 91263 91543 91190 91191 90907 91265 91416 99127 99255 99018 91355 91419 98814 91369 91222 91291 99274 99005 91376 91081 98855 91264 98788 90906 91325 91256 91038
Distribution pattern 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[27620]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 7
SOMATOM Spirit(Model 10045692 )
Z-2478-2018
Recall number Z-2478-2018
Initiated February 01, 2018
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
Device software or design
reason.device_software_design · v1.0.0
software issue
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-2478-2018
Source locator 0001-device-recall-0001-of-0001.json.zip#results[34145]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall A potential risk of unnecessary radiation exposure due to a software issue
Code information Serial No. 31621 31245 79670 31092 31313 31611
Distribution pattern 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[27792]
FDA event record
· Exact recall-number query on openFDA
