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Wolf X-Ray

Flow X Ray Corporation · Model 10005 · UDI-DI 00843696119577

EAM
10
510(k) clearances
0
Adverse events
4
Recalls
9
Facilities

Description

Intensifying Screen, Detail Speed, 10" X 12"

Recalls

DateFirmReason
2004-03-30General Electric Med SystemsThe ball joint that attaches the single monitor platform to the system boom could fail causing the monitor to fall.
2004-03-30General Electric Med SystemsThe ball joint that attaches the single monitor platform to the system boom could fail causing the monitor to fall.
2004-03-30General Electric Med SystemsThe ball joint that attaches the single monitor platform to the system boom could fail causing the monitor to fall.
2004-03-30General Electric Med SystemsThe ball joint that attaches the single monitor platform to the system boom could fail causing the monitor to fall.

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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.