Product Wiki · Recalls · Health Canada — Medical Devices

Plum Lifecare 5000, Plum XL, and Plum XL 3 Infusion Systems and Plum… — recall 51273

Health Canada — Medical Devices · Canada · 2014-03-27 · Type I

As described by Health Canada — Medical Devices: Plum Lifecare 5000, Plum XL, and Plum XL 3 Infusion Systems and Plum XLM with Data Port (2014-01-27)

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
51273
Date of alert
2014-03-27
Country / jurisdiction
Canada
Risk level
Type I
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: The door roller assembly on the Plum Lifecare 5000 series and Plum XL Infuser families has the potential to break which can lead to possible unrestricted flow and/or overdelivery when the door of the pump is opened.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/plum-lifecare-5000-plum-xl-and

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.