Official recall record
20/30 Priority Pack Accessory Kit With Copilot and 20/30 Indeflator Inflation Device
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-11-21
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
This action is being taken due to an increased potential for a leak in the indeflator at the hose rotating luer or at the guage. Analysis indicates an estimated rate of occurrence of leaks ranging from 0.3% to 2.3% across the impacted lots. While no adverse patient effects have been reported with this issue, potential risks include air embolism. Recall Start Date: November 6, 2024
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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