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Med-Rx Medication/Primary Solution Administration Kit — recall 74495

Health Canada — Medical Devices · Canada · 2023-10-30 · Type I

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Agency: Health Canada — Medical Devices
Recall identifier: 74495
Date of alert: 2023-10-30
Country / jurisdiction: Canada
Risk level: Type I
Risk type: recall
Product category: General hospital and personal use
Product type: Medical devices

Reported risk: CHS initiated this recall after receiving a recall letter from Baxter which stated that: "This action is being taken as a precautionary measure as there may be a potential for leaking or dislodged membrane ports on the solution bags during the spiking process when the administration port (spiking port) is used." Recall start date: October 5, 2023

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/med-rx-medicationprimary-solut

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.

Med-Rx Medication/Primary Solution Administration Kit — recall 74495

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