CLASS II ONGOING Device recall · Reported 3 Jul 2024 · FDA Enforcement Report
Axiom Multix MP - Inended Radiographic X ray Table recalled
Siemens Medical Solutions USA is recalling Axiom Multix MP - Inended Radiographic X ray Table is a patient table used in conjunction, distributed nationwide in the US. The recall was initiated on 31 May 2024 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2183-2024
- FDA event ID
- 94777
- Recalling firm
- Siemens Medical Solutions USA, Malvern, PA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 31 May 2024
- FDA classified
- 25 Jun 2024
- Reported
- 3 Jul 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Device type
- Imaging Equipment
Timeline
| 31 May 2024 | Recall initiated by company | |
| 25 Jun 2024 | Classified by FDA | +25 days |
| 3 Jul 2024 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Product as listed by the FDA
AXIOM MULTIX MP - Inended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395431
Where it was distributed
US Nationwide distribution.
Questions about this recall
Why was it recalled?
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Which lots are affected?
UDI-DI: N/A Serial Numbers: 1004 1006 1051 1062 1172 1173 1175 1179 1180 1181 1184 1186 1187 1193 1198 1200 1202 1204 1205 1206
Where was it sold?
US Nationwide distribution.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
8 other products · FDA event 94777This product is part of a recall event; the main page for the event is Axiom Vertix MD - The Vertix MD Trauma has been specially recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Axiom Vertix MD - The Vertix MD Trauma has been specially recalled | Siemens Medical Solutions USA | Other | Nationwide | |
| CLASS II | Multix TOP recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Other | Nationwide | |
| CLASS II | Multix TOP recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Other | Nationwide | |
| CLASS II | Axiom Multix MP - Intended Radiographic X ray Table recalled | Siemens Medical Solutions USA | Other | Nationwide | |
| CLASS II | Axiom Vertix Solitaire - The Vertix MD Trauma has been recalled | Siemens Medical Solutions USA | Other | Nationwide | |
| CLASS II | Axiom Multix MT - Intended Radiographic X ray Table recalled | Siemens Medical Solutions USA | Other | Nationwide | |
| CLASS II | Axiom Multix MT - Intended Radiographic X ray Table recalled | Siemens Medical Solutions USA | Other | Nationwide | |
| CLASS II | ZE for Vertix Solitaire - The Axiom Vertix Solitaire recalled | Siemens Medical Solutions USA | Other | Nationwide |
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