Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
IMPAX RIS QDOC 5.8 Recalled by AGFA Corp. Due to Patient name displayed (printed) on the Patient Report...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact AGFA Corp. directly.
Affected Products
IMPAX RIS QDOC 5.8
Quantity: 14
Why Was This Recalled?
Patient name displayed (printed) on the Patient Report was the wrong patient name.
Where Was This Sold?
This product was distributed to 9 states: CA, FL, GA, ME, OH, OR, SC, SD, TX
About AGFA Corp.
AGFA Corp. has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report