Camera, X-Ray, Fluorographic, Cine Or Spot

Name: Camera, X-Ray, Fluorographic, Cine Or Spot (FDA product code IZJ) — devices, recalls & adverse events
Creator: U.S. Food & Drug Administration

FDA product code IZJ · Class 2 · Radiology

Registered devices

Adverse events

Recalls

510(k) clearances

Recent recalls

Date	Firm	Reason
2013-12-04	Philips Medical Systems (Cleveland) Inc	The recalling firm determined that visual inspections of the fork joints behind the detector that are conducted during six month preventive maintenance (PM) may
2008-05-23	Philips Medical Systems North America Co. Phillips	X-ray images may be stored in the wrong patient file or corrupted, images from two different patients may be combined in one patient's folder or may be combined

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 key Read the docs

Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.