Product Wiki · Recalls · Health Canada — Medical Devices

Zoom Latitude Programmer/Recorder/Monitor (2019-08-21) — recall 44606

Health Canada — Medical Devices · Canada · 2019-08-30 · 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 →
Agency
Health Canada — Medical Devices
Recall identifier
44606
Date of alert
2019-08-30
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Improper software configuration. There were some required software patches that were excluded and some that had extra software added. The improper software is only applicable to certain older pulse generator families, which have not been distributed for over 5 years. The improper software configuration was identified during an internal inspection process. There is no patient risk and no patient harm has been reported to date or is likely to occur.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/zoom-latitude-programmerrecord

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.

Related

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.