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Terminated

Curix Ultra UV-L Plus, Medical Screen Film, X-ray Film, 14x17, 100 Sheet Box

FDA Recall Z-0755-06 · Posted 2006-04-11

Recalling FirmAGFA Corp.
Recall StatusTerminated
Product CodeJAC
Date Initiated2006-02-16
Date Terminated2006-06-22
Product Quantity712 stacks (total includes all types of film)

Reason for Recall

A localized fog pattern appears on the film.

Firm Action

Consignees were notified by telephone on 02/16/2006.

Root Cause

Other

Distribution Pattern

AL, AZ, CA, CO, FL, GA, IN, MA, MI, NC, NJ, NY, OR, SC, TN, TX, WA, VA and Canada

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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