Atlas FDA

Mamoray HDR-C PLUS Mammography film

FDA device recall Z-0788-06 · posted 2006-04-22 · Terminated

Recall details

Recalling firm
AGFA Corp.
Reason for recall
The film was incorrectly notched.
Action taken
Consignees were notified by letter on/about 02/16/2006.
Root cause
Other
Status
Terminated
Product code
IWZ
Quantity affected
16523 units
Distribution
Nationwide
Date initiated
2006-02-16
Date posted
2006-04-22
Date terminated
2006-06-23
Location
Greenville, SC

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