Food, drugs, devices › AGFA Corp.
Device recall: IMPAX RIS QDOC 5.8
AGFA Corp. (Greenville, SC) initiated this device recall on 8 Jan 2014; FDA lists 1 product record under event 67275, classified Class II.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 91% of the 1,176 device enforcement events initiated in 2014 carry the same class.
Status: Terminated, terminated 28 Feb 2014. Initiation: voluntary: firm initiated. AGFA Corp. has 11 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
AGFA Corp., Greenville, SC.
Reason for recall
"Patient name displayed (printed) on the Patient Report was the wrong patient name."
Distribution
"CA, FL, GA, ME, OH, OR, SC, SD, TX and Canada"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-0919-2014 | IMPAX RIS QDOC 5.8 | 14 | Class II | Terminated | 12 Feb 2014 |
Context
Other enforcement events for AGFA Corp.
Questions and answers
Why was this device recalled?
FDA's record gives the reason for recall as: "Patient name displayed (printed) on the Patient Report was the wrong patient name."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "CA, FL, GA, ME, OH, OR, SC, SD, TX and Canada"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 28 Feb 2014. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA device enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.