Device recall: ARTIS One Angiographic X-Ray System
Class II FDA enforcement event 96088. Recall start date: . Status in the FDA record: Ongoing.
Reason for recall, in the words of FDA
A potential issue with ARTIS One systems was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect copper prefiltration. If the described issue occurs, the applied radiation dose-rate may be higher than intended by the user.
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
SIEMENS MEDICAL SOLUTIONS USA, INC started this device recall on 2 Jan 2025. The firm address in the FDA record is in Malvern. FDA put the recall in Class II. FDA event 96088 has 1 product record. The first FDA enforcement report date is 5 Feb 2025. The record gives the status Ongoing.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
23 Distributed in the US
Recalling firm
SIEMENS MEDICAL SOLUTIONS USA, INC, Malvern, Germany.
Recalling firm: The firm that the FDA record names for a recall.
Products
1 product record in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-0922-2025 | ARTIS One Angiographic X-Ray System | 1140 | Class II | Ongoing | 5 Feb 2025 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Device events that started in 2025
- 945
- Share of these events in Class II
- 85%
- Product records in this event
- 1Median of the firm: 1
- Events of the firm on the register
- 400
Other events of the firm
Official channels
- FDA enforcement report Z-0922-2025The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
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Cite this page
Recall Register. FDA enforcement event 96088. https://recallregister.com/fda/ii/96088/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA device enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
23 Distributed in the US
- What quantity of product is in FDA event 96088?
- The FDA record gives this quantity:
1140
- How many device recalls of 2025 have the same class?
- 85% of the 945 device events that started in 2025 are in Class II.
- How many FDA recalls does SIEMENS MEDICAL SOLUTIONS USA, INC have?
- SIEMENS MEDICAL SOLUTIONS USA, INC is the recalling firm in 400 enforcement events on this register. This event is 1 of them.