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FDA Medical Device Recalls (openFDA)

Siemens Medical Solutions USA, Inc: Luminos dRF Max (VE10, VF10, VF11)

Recall number
Z-1480-2023
Recalling firm
Siemens Medical Solutions USA, Inc
Product
Luminos dRF Max (VE10, VF10, VF11)
Status
Open, Classified
Initiated
2022-11-23
Posted
2023-05-23
Terminated
not on file
Reason
Under certain unlikely circumstances during a fluoroscopic examination, the imaging system Fluorospot Compact might sporadically display an incorrect air kerma/air kerma rate related to the patient reference point, according to IEC 60601-2-43. There is no impact on workflow or diagnosis. The error can occur only in fluoroscopy systems with a second (overhead) X-ray tube.
Root cause
Radiation Control for Health and Safety Act
Action
Siemens Medical Solutions USA, Inc., will provide software updates to the affected systems with software versions VF10 and VF11 with software via Update Instructions (UI) XP007/23/S, XP004/23/S, XP003/23/S, and XP001/23/S
Quantity
704 units in the United States (1945 units worldwide)
Distribution
US Nationwide - Worldwide Distribution
Lot, serial or model codes
Model: 10762471
510(k) numbers
["K173639"]
PMA numbers
not on file
Product code
OWB
Firm FEI
2240869
Firm city
Malvern
Firm state
PA
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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