Bard Dynamic Deca Steerable Diagnostic EP Catheter and Daig Livewire Steerable Diagnostic EP Catheter
Brand(s)
Last updated
Summary
Product
Bard Dynamic Deca Steerable Diagnostic EP Catheter and Daig Livewire Steerable Diagnostic EP Catheter
Issue
Medical devices - Sterility
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 |
|---|---|---|
| Bard Dynamic Deca Steerable Diagnostic EP Catheter | More than 10 numbers, contact manufacturer. | 201101 |
| Daig Livewire Steerable Diagnostic EP Catheter | More than 10 numbers, contact manufacturer. | 401904 |
| Daig Livewire Steerable Diagnostic EP Catheter | More than 10 numbers, contact manufacturer. | 401575 |
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.
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies
| Stryker Sustainability Solutions |
| 1810 West Drake Dr., Tempe, Arizona, United States, 85283 |
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-81899
Get notified
Receive emails about new and updated recall and safety alerts.