Official recall record

BD Alaris™ EtCO2, PCA, Syringe, and Pump Modules

Health Canada — Medical Devices · 2024-08-30 · CanadaType II

Issuing authority: Health Canada — Medical Devices
Published: 2024-08-30
Country of alert: Canada
Alert level: Type II
Alert type: recall

What the authority reported

BD has identified an increase in bent contacts on new Female/Left IUI connectors on devices and spare parts manufactured between Jan 01, 2023 and June 06, 2024. BD was made aware of this issue through complaints identified during the device check-in process and has not received any reports of this issue occurring during patient use. A defective pin on certain Female/Left IUI connectors that are not detected prior to use could result in an inoperable device or an operable device where adjoining device cannot be powered on at start up. Recall Start Date: August 15, 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.

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