Exact FDA event identifier

Event 67275

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket: January 08, 2014
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: AGFA Corp.

Dossier provenance

Source snapshots represented here

openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

IMPAX RIS QDOC 5.8

Z-0919-2014

Recall number: Z-0919-2014
Initiated: January 08, 2014
Classification: Class II
Status: Terminated
Recalling firm: AGFA Corp.
Quantity: 14

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Patient name displayed (printed) on the Patient Report was the wrong patient name.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Patient name displayed (printed) on the Patient Report was the wrong patient name.

Code information

Software IMPAX RIS 58 and higher

Distribution pattern

CA, FL, GA, ME, OH, OR, SC, SD, TX and Canada