GVI Technology Partners CDLCAM, First-Pass Radionuclide Angiography Camera System, Model 70-500101, with operating Software Version B1A, marketed by CDL Medical Tech. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
CDLCAM, First-Pass Radionuclide Angiography Camera System, Model 70-500101, with operating Software Version B1A, marketed by CDL Medical Tech.
Brand
GVI Technology Partners
Lot Codes / Batch Numbers
S/Ns: 100 thur 105, and 107 thru 116.
Products Sold
S/Ns: 100 thur 105, and 107 thru 116.
GVI Technology Partners is recalling CDLCAM, First-Pass Radionuclide Angiography Camera System, Model 70-500101, with operating Software due to Due to limitations in the operating software, the acquired scan may not be processed properly.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Due to limitations in the operating software, the acquired scan may not be processed properly.
Recommended Action
Per FDA guidance
The firm notified their distributor by letter on 1/16/2004, software upgrade will be installed on each unit.
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