Medical device shortage: Alaris SmartSite Needle-free System Multi-Way Connecting Set (Infusion Pump Accessory)

The Alaris SmartSite Needle-free System Multi-Way Connecting Set (Infusion Pump Accessory) is currently reported as a medical device shortage through Interim Order No. 2 Respecting Drugs, Medical Devices and Foods for a Special Dietary Purpose in Relation to COVID-19. Interim Order No. 2 repeals and replaces the Interim Order Respecting Drugs, Medical Devices and Foods for a Special Dietary Purpose in relation to COVID-19 (the previous interim order) made by the Minister on March 30, 2020. For a full list of shortages, refer to the list of medical device shortages.

Date published: April 23, 2021

Type of report

Actual medical device shortage

Name of medical device (including any component, accessory or part that is in shortage, including the model name) if applicable

Alaris SmartSite Needle-free System Multi-Way Connecting Set (Infusion Pump Accessory)

Other names (for example trade name), if applicable

n/a

Package description (for example, packaging formats, sizes, quantities)

60 per case

Class of medical device (I, II, III or IV), if known

Class II

Device identifier(s) (for example, serial number, catalogue number, part number, model number or unique device identifier)

2305E; 2306E

Medical device licence number (for Class II, III and IV), if applicable

82625

Authorization identification number (for devices authorized for importation or sale under an interim order made under section 30.1 of the Food and Drugs Act), if applicable

n/a

Single-use product

Yes

Importers that have reported the shortage (Names of importers listed who have reported the shortage separately from the manufacturer or who are reporting on behalf of the manufacturer in a delegated capacity), if applicable

Becton Dickinson Canada Inc.

Manufacturer's name

BD Switzerland Sarl

Manufacturer's mailing address

Business Park Terre-Bonne, Batiment A4
Route De Crassier 17
1262 Eysins
Switzerland

Reason for shortage

Device was subject to a recall

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