Health product recall

BioFlo Dialysis Catheter With Endexo Technology

Last updated

Summary

Product
BioFlo Dialysis Catheter With Endexo Technology
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 catalogue number
BioFlo Dialysis Catheter With Endexo Technology All lots. H965103028041
BioFlo Dialysis Catheter With Endexo Technology All lots. H965103028051
BioFlo Dialysis Catheter With Endexo Technology All lots. H965103028061
BioFlo Dialysis Catheter With Endexo Technology All lots. H965103028070
BioFlo Dialysis Catheter With Endexo Technology All lots. H965103028090
BioFlo Dialysis Catheter With Endexo Technology All lots. H965103028080
BioFlo Dialysis Catheter With Endexo Technology All lots. H965103028031

Issue

Merit Medical Systems, Inc. (Merit) is conducting a voluntary recall of the Merit 16F Dual-valved Splittable Sheath Introducer due to a design defect. Specifically, the sheath introducer may not split as intended. This sheath introducer is used in several Merit finished devices (e.g. BioFlo DuraMax catheter).

Merit has received customer complaints related to this issue, some of which involve patient injury. Failure of the sheath introducer to split as intended may result in hemorrhage, foreign bodies, and procedure delay.

Merit is requesting customers to immediately discontinue the use of the 16F dual-valved splittable sheath introducer and destroy the sheath introducer at point of use. The other products included with the sheath introducer may continue to be used.

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Gastroenterology and urology
Companies
Merit Medical Systems Inc.
1600 West Merit Parkway, South Jordan, Utah, United States, 84095
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-81625

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