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FUJI MEDICAL DRY FILM
FUJIFILM CORPORATION · Model DI-HT 35X43 100 · UDI-DI 04547410080797
LMC
Prescription
1
510(k) clearances
6
Adverse events (2 deaths)
3
Recalls
19
Facilities
Description
MEDICAL DRY IMAGING FILM 100NIF 35x43
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-03-11 | Philips Medical Systems (Cleveland) Inc | The firm was notified by a customer that the collimator exchange carriage and the collimator storage cabinet were misaligned. |
| 2008-05-16 | AGFA Corp. | The "Film Calibration" setting on the printers was set to the default "OFF" position instead of "ON". |
| 2003-11-25 | AGFA Corp. | The GS1 circuit board may fail resulting in smoke or fire. |
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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.