Product Wiki · Recalls · Health Canada — Medical Devices

Unicel Dxh Slidemaker Stainer Coulter Cellular Analysis System — recall 56987

Health Canada — Medical Devices · Canada · 2017-07-17 · 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
56987
Date of alert
2017-07-17
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: Beckman Coulter has determined that a fitting installed in a select population of Slidemaker Stainer (SMS) units may not completely seal after being installed. Not all fittings installed may be affected. For those affected, one may observe a slow dripping leak of the staining reagents (methanol, alcohol and buffers) into the spill tray below designed for this purpose.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/unicel-dxh-slidemaker-stainer-

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.