Health product recall

BLUSelect®, BLUgriggs® and BLUperc® Products

Last updated

Summary

Product
BLUSelect®, BLUgriggs® and BLUperc® Products
Issue
Medical devices - Performance issue
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

BLUgriggs Percutaneous Dilation Tracheostomy Kit

More than 10 numbers, contact manufacturer.

101/541/080

BLUperc Percutaneous Dilation Tracheostomy Kit

More than 10 numbers, contact manufacturer.

101/563/080
101/563/070
101/561/080
101/561/090
101/561/070

BLUSelect Tracheostomy Tubes

More than 10 numbers, contact manufacturer.

101/815/075
101/815/090
101/817/080
101/817/060
101/817/090
101/875/060
101/815/070
101/815/100
101/875/070
101/815/080
101/817/070
101/875/090
101/875/080
101/875/085
101/815/060
101/815/085
101/875/075

Issue

Smiths Medical has identified the potential for a disconnection of the pilot balloon from the tracheostomy inflation line within specific lots of the BLUSelect®, BLUgriggs® and BLUperc® products because of a manufacturing defect.

Recall Start Date: June 3, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Anaesthesiology
Companies

Smiths Medical Asd, Inc.

6000 Nathan Lane N., Minneapolis, Minnesota, United States, 55442

Published by
Health Canada
Audience
Healthcare
Recall class
Type I
Identification number
RA-75653

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