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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