Home › I.A.E. INDUSTRIA APPLICAZIONI ELETTRONICHE SPA › RTM 102 H
RTM 102 H
I.A.E. INDUSTRIA APPLICAZIONI ELETTRONICHE SPA · Model 0.6/1.5 · UDI-DI 08059307490948
ITY
Prescription
10
510(k) clearances
55
Adverse events
4
Recalls
54
Facilities
Description
Rotating anode X-ray tube for radiography systems
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-04-07 | Dunlee | The x-ray tube housing assembly may have been mounted with the incorrect sized bolts. |
| 2005-04-07 | Dunlee | The x-ray tube housing assembly may have been mounted with the incorrect sized bolts. |
| 2005-04-07 | Dunlee | The x-ray tube housing assembly may have been mounted with the incorrect sized bolts. |
| 2004-04-12 | Fischer Imaging Corporation | X-ray tube may overheat after high usage because of mis-wired thermal switch circuit. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.
