Agfa Cronex 10T Radiographic film
FDA Recall Z-0471-06 · Posted 2006-02-04
Recalling FirmAGFA Corp.
Recall StatusTerminated
Product CodeJAC
Date Initiated2005-12-21
Date Terminated2006-04-18
Product Quantity118 boxes
Reason for Recall
Mislabeling; Product labeled Cronex 10T actually contains Afga, Curix Ultra UVL Plus.
Firm Action
Consignees were first contact by telephone followed up with a certified letter, on/about 12/21/2005.
Root Cause
Other
Distribution Pattern
AZ, CA, CO, GA, IL, MI, NE, NV, OH, OR, WA and Canada
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.