Product Wiki · Recalls · Health Canada — Medical Devices

BD Alaris™ EtCO2, PCA, Syringe, and Pump Modules — recall 75992

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

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Agency
Health Canada — Medical Devices
Recall identifier
75992
Date of alert
2024-08-30
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
General hospital and personal use
Product type
Medical devices
Reported risk: 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
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/bd-alaristm-etco2-pca-syringe-

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.

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