Z-0755-06

Curix Ultra UV-L Plus, Medical Screen Film, X-ray Film, 14x17, 100 Sheet Box

Name: Z-0755-06 Curix Ultra UV-L Plus, Medical Screen Film, X-ray Film, 14x17, 100 Sheet Box
Creator: AGFA Corp.
Published: 2006-02-16
License: https://open.fda.gov/license/

AGFA Healthcare Corp. / initiated 2006-02-16 / Terminated

FDA source

AGFA Corp. began a recall of Curix Ultra UV-L Plus, Medical Screen Film, X-ray Film, 14x17, 100 Sheet Box on 2006-02-16. The reason FDA records is "A localized fog pattern appears on the film". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0755-06
Status: Terminated
Initiated: 2006-02-16
Posted: 2006-04-11
Terminated: 2006-06-22
Recalling firm: AGFA Healthcare Corp.
Product: Curix Ultra UV-L Plus, Medical Screen Film, X-ray Film, 14x17, 100 Sheet Box
Product code: JAC System, X-Ray, Film Marking, Radiographic
Reason for recall: A localized fog pattern appears on the film.
FDA root cause: Other
Action: Consignees were notified by telephone on 02/16/2006.
Quantity in commerce: 712 stacks (total includes all types of film)
Distribution: AL, AZ, CA, CO, FL, GA, IN, MA, MI, NC, NJ, NY, OR, SC, TN, TX, WA, VA and Canada
Product codes and lots: Product Code; EKQEG, Manufacturing Batch or Lot: 79340029

Product code JAC

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)