Public recall detail

Bard Dynamic Deca Steerable Diagnostic EP Catheter and Daig Livewire Steerable Diagnostic EP Catheter

2026-04-15

medium
Cardiovascular Sterility
Quick summary

Quick summary: Bard Dynamic Deca Steerable Diagnostic EP Catheter and Daig Livewire Steerable Diagnostic EP Catheter. Reason: Sterility. Category: Cardiovascular. Date: 2026-04-15.

Recommended action

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

Recall details

Quick summary: Bard Dynamic Deca Steerable Diagnostic EP Catheter and Daig Livewire Steerable Diagnostic EP Catheter. Reason: Sterility. Category: Cardiovascular. Date: 2026-04-15.

Official details

Affected product details

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

BrandStryker Sustainability Solutions
ProductBard Dynamic Deca Steerable Diagnostic EP Catheter and Daig Livewire Steerable Diagnostic EP Catheter
IssueMedical devices - Sterility
Recall classType II
IdentificationRA-81899

Affected products

ProductBard Dynamic Deca Steerable Diagnostic EP Catheter
LotMore than 10 numbers, contact manufacturer.
Model201101
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionBard Dynamic Deca Steerable Diagnostic EP Catheter
ProductDaig Livewire Steerable Diagnostic EP Catheter
LotMore than 10 numbers, contact manufacturer.
Model401904
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionDaig Livewire Steerable Diagnostic EP Catheter
ProductDaig Livewire Steerable Diagnostic EP Catheter
LotMore than 10 numbers, contact manufacturer.
Model401575
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionDaig Livewire Steerable Diagnostic EP Catheter

Issue

Stryker Sustainability Solutions (SSS) has received complaints reporting EP catheter devices with breached sterile barriers on the chevron seal side of the primary Tyvek pouch.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Cardiovascular
CompaniesStryker Sustainability Solutions 1810 West Drake Dr., Tempe, Arizona, United States, 85283
Recall date2026-04-08
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-81899
Background{}
CompaniesStryker Sustainability Solutions 1810 West Drake Dr., Tempe, Arizona, United States, 85283
AudiencesHealthcare
Source updated2026-04-15

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

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