Agfa Cronex 10T Radiographic film
FDA device recall Z-0471-06 · posted 2006-02-04 · Terminated
Recall details
- Recalling firm
- AGFA Corp.
- Reason for recall
- Mislabeling; Product labeled Cronex 10T actually contains Afga, Curix Ultra UVL Plus.
- Action taken
- Consignees were first contact by telephone followed up with a certified letter, on/about 12/21/2005.
- Root cause
- Other
- Status
- Terminated
- Product code
- JAC
- Quantity affected
- 118 boxes
- Distribution
- AZ, CA, CO, GA, IL, MI, NE, NV, OH, OR, WA and Canada
- Date initiated
- 2005-12-21
- Date posted
- 2006-02-04
- Date terminated
- 2006-04-18
- Location
- Greenville, SC
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