Product Wiki · Recalls · Health Canada — Medical Devices

AMSCO V-PRO 60 LOW TEMPERATURE STERILIZATION SYSTEM (2017-10-12) — recall 57995

Health Canada — Medical Devices · Canada · 2017-11-24 · 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
57995
Date of alert
2017-11-24
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: STERIS has become aware that the V-PRO 60 software verifies expiration date of the Vaprox Sterilant upon completion of the sterilization cycle rather than prior to cycle initiation. Verification of the Vaprox expiration date at the end of the sterilization cycle will allow for the completion of one cycle with expired Vaprox Sterilant.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/amsco-v-pro-60-low-temperature

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.