Recall archive / FDA device enforcement
Artis icono biplane- Model No. 11327600 Artis icono floor- Model No. 11327700 — FDA record Z-1647-2022
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Aug 10, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Artis icono biplane- Model No. 11327600 Artis icono floor- Model No. 11327700
- Reason
- Siemens has become aware of a potential hardware issue with Artis Q, Artis Q.zen, Artis pheno and Artis icono systems with a specific lot of X-ray tubes. In rare cases, if the error detection mechanism fails, it will not be possible to release X-ray any longer until system shutdown.
- Classification
- Class II
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 1,389 (590 US; 799 OUS) (Total)
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1647-2022
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Artis icono biplane- Model No. 11327600 UDI-DI: 04056869063317 Serial Numbers 180062 180054 180019 180421 180444 180034 180072 180446 180367 180438 180382 180060 180428 180369 180370 180371 180372 180080 180301 180305 180067 180399 180442 180040 180379 180386 180360 180333 180352 180407 180433 180412 180400 180397 180432 180316 180447 180363 180429 180084 180418 180334 180018 180376 180354 180046 180434 180357 180358 180361 180362 180081 180423 180411 180414 180381 180021 180443 180309 180356 180378 180393 180368 180413 180323 180439 180445 180430 180043 180437 180049 180377 180077 180055 180014 180037 180373 ***Updated 9/23/22*** 180466 180465 180464 180047 180463 ***Updated 1/9/23*** 180470 180534 180468 180472 180467 180469 180066 180082 Artis icono floor- Model No. 11327700 UDI-DI: 04056869149325 Serial Numbers 170319 170391 170392 170397 170026 170388 170343 170367 170368 170360 170349 170361 170383 170322 170385 170386 170025 170384 170346 170051 170358 170389 170357 170365 170387 170390 170393 170394 170378 170396 170053 170364 ***Updated 1/9/23*** 170402 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Worldwide Distribution: US (nationwide) and OUS (Foreign) to countries of: United Arab Emirates; Armenia; Angola; Argentina; Austria; Australia; Bangladesh; Belgium; Bulgaria; Bahrain; Brazil; Canada; Switzerland; China; Colombia; Costa Rica; Czech Republic; Germany; Denmark; Dominican Republic; Algeria; Estonia; Egypt; Spain; Finland; France; United Kingdom; Greece; Guatemala; Hong Kong; Croatia; Inhouse Company; Indonesia; Ireland; Israel; India; Iran; Italy; Jordan; Japan; South Korea; Kuwait; Kazakhstan; Lebanon; Luxembourg; Monaco; Mongolia; Martinique; Mexico; Malaysia; Netherlands; Norway; New Zealand; Oman; Philippines; Poland; Portugal; Qatar; Serbia; Russian Federation; Saudi Arabia; Sweden; Singapore; Slovenia; Slovakia; El Salvador; Thailand; Turkey; Taiwan; Ukraine; Vietnam and South Africa.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Report date
- Sep 7, 2022
- Recall initiation date
- Aug 10, 2022
- Center classification date
- Aug 26, 2022
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.