FDA Device recall Z-2474-2018
SOMATOM Perspective (Model 10495568)
- FDA Device
- Class II
- terminated
- Published 2018-08-08
On 2018-08-08 the FDA classified a Class II recall of SOMATOM Perspective (Model 10495568) by Siemens Medical Solutions Usa, citing A potential risk of unnecessary radiation exposure due to a software issue.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2474-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-02-01 |
| Published | 2018-08-08 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
SOMATOM Perspective (Model 10495568)
Reason
A potential risk of unnecessary radiation exposure due to a software issue
Identifiers
| code_info | Serial No. 59298 59019 59195 59686 59060 59045 59050 59223 59038 59024 59052 59182 59041 59251 77649 12…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 593 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2474-2018%22
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