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[Recalled] BD Alaris™ Infusion Devices — Device compatibility | Health Canada 2023-10-30
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | BD Alaris™ Infusion Devices |
|---|---|
| Category | General hospital and personal use |
| Issuing authority | HC |
| Reference | 74491 |
| Country of notice | Canada |
| Risk level | Type I |
| Hazard type | recall |
| Notice date | 30 October 2023 |
Why it was recalled
According to the HC notice, the identified hazard is: Device compatibility
This Type I recall concerns General hospital and personal use products distributed in Canada and was recorded by HC. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Review the official notice to confirm whether your unit is affected.
Read the full official notice →
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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