Product Wiki · Recalls · Health Canada — Medical Devices

LMA Mucosal Atomization Devices — recall 55783

Health Canada — Medical Devices · Canada · 2016-11-18 · 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: 55783
Date of alert: 2016-11-18
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: Medical devices
Product type: Medical devices
Notice status: Archived by the issuing authority — kept for reference

Reported risk: Teleflex is recalling these products as they may produce a straight stream instead of a fully atomized plume of medication. This may result in inadequate topical anesthesia which may lead to some discomfort, further attempts to deliver topical anesthesia, or the use of alternative methods of anesthesia.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/lma-mucosal-atomization-device

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.

LMA Mucosal Atomization Devices — recall 55783

Related