AGFA Corp. CR DX-S, Image Intensified Fluoroscopic X-ray system. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
CR DX-S, Image Intensified Fluoroscopic X-ray system.
Brand
AGFA Corp.
Lot Codes / Batch Numbers
Units with Serial number SN1001- SN1179, and SN1181, SN1183 and SN1184, Software versions: STR_1207 and below.
Products Sold
Units with Serial number SN1001- SN1179, and SN1181, SN1183 and SN1184; Software versions: STR_1207 and below.
AGFA Corp. is recalling CR DX-S, Image Intensified Fluoroscopic X-ray system. due to Three separate issues involving the Agfa DX-S CR System, were detected that could lead to an image loss.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Three separate issues involving the Agfa DX-S CR System, were detected that could lead to an image loss.
Recommended Action
Per FDA guidance
Consignees were notified by letter on/about 06/28/2006.
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
CA, FL, MI, MN, MS, OR, DC
Page updated: Jan 10, 2026