Data Foundry

Medical device recalls 2024

MULTIX TOP — Class II medical device recall Z-2186-2024

Ongoing recall by Siemens Medical Solutions USA, Inc, reported 2024-07-03, distributed nationwide. Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire

Recall numberZ-2186-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmSiemens Medical Solutions USA, Inc, Malvern, PA, United States
Recall initiated2024-05-31
Classified2024-06-25
Reported by FDA2024-07-03
DistributedNationwide (US)
Quantity3 units
Reason classesdevice malfunction
Serial numbers1004, 1006, 1011, 1014

Product

MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number:475517

Reason for recall

Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2186-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.