ARIES and ARIES M1 System (2018-07-02) — recall 58086
Health Canada — Medical Devices · Canada · 2018-07-13 · Type II
🏛Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Reported risk: A potential discrepancy in the firmware for a subset of ARIES System Barcode Scanners (CN-0321-01). When the potentially affected barcode scanner is used on multiple ARIES Cassettes at the same time, the system may prepopulate the "sample id" field with a previously stored sample id.
Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.
ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.