Public recall detail

BioFlo Dialysis Catheter With Endexo Technology

2026-02-19

medium
Gastroenterology and urology Performance
Quick summary

Quick summary: BioFlo Dialysis Catheter With Endexo Technology. Reason: Performance. Category: Gastroenterology and urology. Date: 2026-02-19.

Recommended action

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.

Official details

Affected product details

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

BrandMerit Medical Systems Inc.
ProductBioFlo Dialysis Catheter With Endexo Technology
IssueMedical devices - Performance
Recall classType II
IdentificationRA-81625

Affected products

ProductBioFlo Dialysis Catheter With Endexo Technology
LotAll lots.
ModelH965103028041
Serial numberAll lots.
DescriptionBioFlo Dialysis Catheter With Endexo Technology
ProductBioFlo Dialysis Catheter With Endexo Technology
LotAll lots.
ModelH965103028051
Serial numberAll lots.
DescriptionBioFlo Dialysis Catheter With Endexo Technology
ProductBioFlo Dialysis Catheter With Endexo Technology
LotAll lots.
ModelH965103028061
Serial numberAll lots.
DescriptionBioFlo Dialysis Catheter With Endexo Technology
ProductBioFlo Dialysis Catheter With Endexo Technology
LotAll lots.
ModelH965103028070
Serial numberAll lots.
DescriptionBioFlo Dialysis Catheter With Endexo Technology
ProductBioFlo Dialysis Catheter With Endexo Technology
LotAll lots.
ModelH965103028090
Serial numberAll lots.
DescriptionBioFlo Dialysis Catheter With Endexo Technology
ProductBioFlo Dialysis Catheter With Endexo Technology
LotAll lots.
ModelH965103028080
Serial numberAll lots.
DescriptionBioFlo Dialysis Catheter With Endexo Technology
ProductBioFlo Dialysis Catheter With Endexo Technology
LotAll lots.
ModelH965103028031
Serial numberAll lots.
DescriptionBioFlo Dialysis Catheter With Endexo Technology

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
AudienceHealthcare
CategoryHealth products - Medical devices - Gastroenterology and urology
CompaniesMerit Medical Systems Inc. 1600 West Merit Parkway, South Jordan, Utah, United States, 84095
Recall date2026-02-05
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-81625
Background{}
CompaniesMerit Medical Systems Inc. 1600 West Merit Parkway, South Jordan, Utah, United States, 84095
AudiencesHealthcare
Source updated2026-02-19

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

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