Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

iVIEW DAB Detecion Kit. Catalog Number 760-091

FDA Recall Z-0928-03 · Posted 2003-06-17

Recalling FirmVentana Medical Systems Inc
Recall StatusTerminated
Product CodeKTO
Date Initiated2003-05-07
Date Terminated2004-05-03
Product Quantity409 kits

Reason for Recall

Kit does not stain tissues properly.

Firm Action

Recall notification was made by telephone on May 6 and 7, 2003. A faxed letter and response form followed.

Root Cause

Other

Distribution Pattern

Nationwide.

Official Source

View FDA Recall →

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

↑