Health product recall

Xps System-Blades

Last updated

Summary

Product
Xps System-Blades
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
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

Get notified

Receive emails about new and updated recall and safety alerts.

Subscribe