Curix Ultra UV-L Plus, Medical Screen Film, X-ray Film, 14x17, 100 Sheet Box
FDA device recall Z-0755-06 · posted 2006-04-11 · Terminated
Recall details
- Recalling firm
- AGFA Corp.
- Reason for recall
- A localized fog pattern appears on the film.
- Action taken
- Consignees were notified by telephone on 02/16/2006.
- Root cause
- Other
- Status
- Terminated
- Product code
- JAC
- Quantity affected
- 712 stacks (total includes all types of film)
- Distribution
- AL, AZ, CA, CO, FL, GA, IN, MA, MI, NC, NJ, NY, OR, SC, TN, TX, WA, VA and Canada
- Date initiated
- 2006-02-16
- Date posted
- 2006-04-11
- Date terminated
- 2006-06-22
- Location
- Greenville, SC
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.