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Med-Rx Medication/Primary Solution Administration Kit — recall 82529

Health Canada — Medical Devices · Canada · 2026-08-26 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 82529
Date of alert: 2026-08-26
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: General hospital and personal use
Product type: Medical devices

Reported risk: CHS was notified by ICU Medical Canada that they are conducting a recall of certain IV sets as discoloration may be present in the drip chamber of the IV sets. ICU Medical IV Tubing Dets with a drip chamber that are within their expiration date are impacted. The products should continue to be used as intended and per facility protocol. CHS Ltd. uses these IV sets in the medical devices they manufacture.

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 82529

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