Intellivue MP and X2 Patient Monitor Systems (2014-04-04) — recall 51147
Health Canada — Medical Devices · Canada · 2014-04-30 · 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 →
Archived by the issuing authority — kept for reference
Reported risk: On-going monitoring of quality data determined that the risk of battery failure increases with age, when a battery remains in use longer than 3 years after the date of manufacture or 5-charge-discharge cycles. Such failure may result in overheating. Battery management and safety practices information for the batteries M4605A/M4607A are not clearly documented in the instructions for use for intellivue patient monitors with software releases up to and including G.0.
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.