HIGH

Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER

Incomplete seals on sterile product

Quick Facts at a Glance

Recall Date
April 10, 2026
Hazard Level
HIGH
Brand
Stryker Sustainability Solutions
Geographic Scope
1 states

Hazard Information

Incomplete seals on sterile product

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Stryker Sustainability Solutions or your healthcare provider for instructions

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Full Description

Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER. Reason: Incomplete seals on sterile product. Classification: Class II. Quantity: 1352 units. Distribution: US Nationwide and the countries of Israel and Canada.

View Original Recall on FDA - Medical Devices

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Product Classification

Product Details

Model Numbers
UDI 00885825007263
Lot Numbers: 3016810
4488621
4592565
4801485
+15 more
Affected States
ALL
Report Date
May 20, 2026
Recall Status
ACTIVE

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