Public recall detail

Rotatable Fusion Blades

2022-08-11

medium
Recall Safety notice
Quick summary

Quick summary: Rotatable Fusion Blades. Date: 2022-08-11.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Rotatable Fusion Blades. Date: 2022-08-11.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandMedtronic Navigation, Inc.
ProductRotatable Fusion Blades
IssueMedical devices - Performance
Recall classType II
IdentificationRA-64447

Affected products

ProductRotatable Fusion Blades
LotMore than 10 numbers, contact manufacturer.
Model1884080EM 1883480EM 1884006EM 1884012EM 1884380EM 1883080EM
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionRotatable Fusion Blades

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

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - General and plastic surgery
CompaniesMedtronic Navigation, Inc. 826 Coal Creek Circle, Louisville, Colorado, United States, 80027
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-64447
Background{}
CompaniesMedtronic Navigation, Inc. 826 Coal Creek Circle, Louisville, Colorado, United States, 80027
AudiencesHealthcare
Source updated2021-09-01

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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