Quick summary: BioFlo Dialysis Catheter With Endexo Technology. Reason: Performance. Category: Gastroenterology and urology. Date: 2026-02-19.
BioFlo Dialysis Catheter With Endexo Technology
2026-02-19
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: BioFlo Dialysis Catheter With Endexo Technology. Reason: Performance. Category: Gastroenterology and urology. Date: 2026-02-19.
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
Affected products
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.
What you should do
- Contact the manufacturer if you require additional information.
Additional official information
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
Frequently asked questions
Answers based on the official recall notice.
Product images
Official product images from Health Canada.
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