Health product recall

Guidewire 70cm X 1mm (0.038 Inch)

Last updated

Summary

Product
Guidewire 70cm X 1mm (0.038 Inch)
Issue
Medical devices - Performance
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

Guidewire 70cm X 1mm (0.038 Inch)

More than 10 numbers, contact manufacturer.

5583705

Issue

BD has received multiple reports that guidewire code 5583705, which is intended for use with the Bard 14.5 Fr Long-Term Dual Lumen Hemodialysis Catheters, may have been misassembled within the hoop such that the proximal (stiff) end of the guidewire is located at the distal end of the hoop.  When loaded correctly the distal (flexible) end of the guidewire should be located at the distal end of the guidewire hoop.

Recall Start Date: August 1, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General and plastic surgery
Companies

Bard Access Systems, Inc.

605 North 5600 West, Salt Lake City, Utah, United States, 84116

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75930

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