Flexiva™ Pulse Tractip™
Brand(s)
Last updated
Summary
Product
Flexiva™ Pulse Tractip™
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 |
|---|---|---|
| Flexiva™ Pulse Tractip™ | More than 25 numbers, contact manufacturer. | M006L8405961 M006L8405960 |
Issue
Boston Scientific Corporation is initiating a removal of specific lots of Flexiva Pulse and Flexiva Pulse Tractip high power single-use laser fibers that were manufactured using an incorrect component located within the fiber connector.
Recall start date: May 25, 2023
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies
Boston Scientific Corporation
300 Boston Scientific Way, Marlborough, Massachusetts, United States, 01752
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-73816
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