Health product recall

Xps System-Blades

Last updated

Summary

Product
Xps System-Blades
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

Xps System-Blades

More than 10 numbers, contact manufacturer.

1883516HRE
1882916
1884380HR
1883080HRE
1883506HRE
1883514
1883480HRE
1884013
1882936E
1884005HRE
1884030HRE
1884033HRE
1882902HRE
1882924HRE
1883502HRE
1883512HRE
1884031HRE
1884032
1882905HRE
1884020

Issue

Medtronic is voluntarily recalling specific lot numbers of sterile blade single-use accessories. Navigation blades are being used to aid in accuracy during the procedure, and if they wobble, that accuracy and precision is diminished. Medtronic has received complaints related to tip breaks and wobble/vibration in this subset of devices. Tip breaks or detachment of fragments may cause harm to the patient, cause lack of oxygenation or foreign body reaction if the fragment were to migrate into the patient's airway or be irretrievable. There is also a chance that the tip may impact critical structures such as nerves and arteries. Blade wobble or vibration may also lead to permanent damage if it causes the blade to impact critical structures.

Recall start date: August 16, 2021

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Ear, nose and throat
Companies

Medtronic Xomed Inc.

6743 Southpoint Drive North, Jacksonville, Florida, United States, 32216

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-64448

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