AGFA Corp. Curix Ultra UV-L Plus, Medical Screen Film, X-ray Film, 14x17, 100 Sheet Box Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Curix Ultra UV-L Plus, Medical Screen Film, X-ray Film, 14x17, 100 Sheet Box
Brand
AGFA Corp.
Lot Codes / Batch Numbers
Product Code, EKQEG, Manufacturing Batch or Lot: 79340029
Products Sold
Product Code; EKQEG, Manufacturing Batch or Lot: 79340029
AGFA Corp. is recalling Curix Ultra UV-L Plus, Medical Screen Film, X-ray Film, 14x17, 100 Sheet Box due to A localized fog pattern appears on the film.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
A localized fog pattern appears on the film.
Recommended Action
Per FDA guidance
Consignees were notified by telephone on 02/16/2006.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AZ, CA, CO, FL, GA, IN, MA, MI, NJ, NY, NC, OR, SC, TN, TX, VA, WA
Page updated: Jan 10, 2026