AGFA Corp. IMPAX CV Results Manager/Results Manager Administration Tool The IMPAX Cardiovascular suite is a cardiovascular information system providing image archiving and image display and modality study-specific structured reporting. The suite is comprised of modular software that runs on industry standard personal computers and servers, utilizing Windows 2000/2003/XP operating systems. Image data storage/display utilizes DICO< (Digital Imaging and Communications in Medicine) data primarily from indepen Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
IMPAX CV Results Manager/Results Manager Administration Tool The IMPAX Cardiovascular suite is a cardiovascular information system providing image archiving and image display and modality study-specific structured reporting. The suite is comprised of modular software that runs on industry standard personal computers and servers, utilizing Windows 2000/2003/XP operating systems. Image data storage/display utilizes DICO< (Digital Imaging and Communications in Medicine) data primarily from indepen
Brand
AGFA Corp.
Lot Codes / Batch Numbers
Software Versions: RM 2.03, 2.04 & 2.06
Products Sold
Software Versions: RM 2.03, 2.04 & 2.06
AGFA Corp. is recalling IMPAX CV Results Manager/Results Manager Administration Tool The IMPAX Cardiovascular suite is a ca due to User could modify a measurement's units and that change would not be reflected in echocardiography formulas used within the Adult echocardiography RM.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
User could modify a measurement's units and that change would not be reflected in echocardiography formulas used within the Adult echocardiography RM.
Recommended Action
Per FDA guidance
The firm, Agfa Healthcare, sent individual letters dating from April 15, 2009 to August 26, 2009, to the customers. The letters described the product, problem and actions to be taken. Agfa provided the affected customer with a complete list of their impacted patients and the measurements. Agfa also scheduled unit corrections with their customers and received acknowledgement of the letters at the time of scheduling the unit corrections. Service Bulletin DIS026.09E was issued January 2009 to inform users that Agfa will no longer allow customers to request unit changes for measurements that have formulas. Note: Technical Support ran diagnostic scripts for each customer and documented in GSC cases for each consignee/customer. If you have any questions, contact Agfa Healthcare at (949) 830-4959.
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 noticePage updated: Jan 10, 2026