FDA Device Intelligence
HomeSHIMADZU CORPORATION › 0.7/1.3U163C-36

0.7/1.3U163C-36

SHIMADZU CORPORATION · Model 582-24780-62 · UDI-DI 04540217059478

ITY
10
510(k) clearances
55
Adverse events
4
Recalls
54
Facilities

Recalls

DateFirmReason
2005-04-07DunleeThe x-ray tube housing assembly may have been mounted with the incorrect sized bolts.
2005-04-07DunleeThe x-ray tube housing assembly may have been mounted with the incorrect sized bolts.
2005-04-07DunleeThe x-ray tube housing assembly may have been mounted with the incorrect sized bolts.
2004-04-12Fischer Imaging CorporationX-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 docs
Data 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.