Product Wiki · Recalls · Health Canada — Medical Devices

EVODIAL 1.3, 1.6, 2.2 and NEPHRAL ST 300, NEPHRAL ST 400, NEPHRAL ST… — recall 44574

Health Canada — Medical Devices · Canada · 2019-05-31 · Type II

As described by Health Canada — Medical Devices: EVODIAL 1.3, 1.6, 2.2 and NEPHRAL ST 300, NEPHRAL ST 400, NEPHRAL ST 500 (2019-05-15)

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
44574
Date of alert
2019-05-31
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Baxter is taking this action as a precautionary measure as these dialyzers were potentially exposed to temperatures below 0 degrees celsius during shipment to canada. There may be a potential for internal blood leakages (IBLS) to occur during therapy with the use of these affected dialyzers.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/evodial-13-16-22-and-nephral-s

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.