FDA Device recall Z-2475-2018
SOMATOM Perspective 16 (Model 10891666)
- FDA Device
- Class II
- terminated
- Published 2018-08-08
On 2018-08-08 the FDA classified a Class II recall of SOMATOM Perspective 16 (Model 10891666) 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-2475-2018 |
| 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 16 (Model 10891666)
Reason
A potential risk of unnecessary radiation exposure due to a software issue
Identifiers
| code_info | Serial No. 87559 87579 87532 87539 87563 87565 87560 87555 87556 87553 87554 87526 87567 87561 87589 87…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 |
|---|
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-2475-2018%22
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