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RoseM
DRTECH Corporation · Model RSM 2430C · UDI-DI 08800018401903
1
510(k) clearances
659
Adverse events (5 deaths)
41
Recalls
42
Facilities
Description
The RSM 2430C is designed for use in Digital X-ray Images of woman breast diagnosis (mammography), which intended to be used in radiographic film/screen systems in general-purpose diagnostic procedures. The system can be applied wherever traditional X-ray screen-film cassettes are currently used.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-04-08 | Hologic, Inc | Complaints have been received of systems developing loose, missing, or broken internal bolts over time. |
| 2025-10-24 | GE Medical Systems, LLC | Some Senographe Pristina systems either have a missing or an incorrect X-Ray Warning label, which is a nonconformance to FDA Regulation 21 CFR 1020.30(j). |
| 2025-10-24 | Siemens Medical Solutions USA, Inc | There were instances where the operator table was sold together with a bus-installation kit. The operator table is not intended and not released for bus installations as it was des |
| 2025-10-24 | Siemens Medical Solutions USA, Inc | There were instances where the operator table was sold together with a bus-installation kit. The operator table is not intended and not released for bus installations as it was des |
| 2025-10-24 | Siemens Medical Solutions USA, Inc | There were instances where the operator table was sold together with a bus-installation kit. The operator table is not intended and not released for bus installations as it was des |
| 2023-12-26 | GE Medical Systems, SCS | X-ray exposure termination audible signal on Senographe Pristina with Efficiency Suite 2 intermittently not emitted per 21CFR 1020.31(j) requirements. |
| 2020-05-07 | Siemens Medical Solutions USA, Inc | If an examination is interrupted when the InSpect Projection View (PV) is active and the vacuum biopsy system is being used, the tube arm's manual movement range is decreased from |
| 2020-01-21 | Hologic, Inc. | The recalling firm has received reports from the field of the C-arm on the Selenia Dimensions system seizing or dropping during field repairs and cleaning of the systems. |
| 2019-07-23 | Siemens Medical Solutions USA, Inc | An error can occur when performing a biopsy using the InSpect function. The acquisition workstation may become unresponsive to normal user interaction, can only take place in rare |
| 2019-05-16 | GE Healthcare, LLC | Potential slippage of the biopsy positioner when the gantry is rotated during a biopsy procedure. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.