Official recall record
BD Texium™ Components
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-05-23
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Through complaint investigations, BD has identified that specific lots of standalone Texium™ components, and IV infusion sets and syringes containing the Texium™ closed-male luer component (as listed in attachment 1) have the potential to leak during use at the connection interface between the Texium™ component and the SmartSite™ needle-free connector. BD has confirmed that this issue is limited to the affected products listed in attachment 1. Recall start date: May 12, 2025
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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