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Daig Livewire Steerable, Product Number 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
April 10, 2026
Status
ACTIVE

Quick Facts at a Glance

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

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Stryker Sustainability Solutions
Model numbers
UDI 00885825006815, Lot Numbers: 2696145, 3794476, 4262195, 4633829, 4786916, 4849947, 5002352 +12 more
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    April 10, 2026

  2. Reported by FDA DEVICE

    May 20, 2026

  3. RecallRadar source check

    May 27, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER. Reason: Incomplete seals on sterile product. Classification: Class II. Quantity: 319 units. Distribution: US Nationwide and the countries of Israel and Canada.

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
UDI 00885825006815
Lot Numbers: 2696145
3794476
4262195
4633829
+15 more
Affected States
ALL
Report Date
May 20, 2026
Recall Status
ACTIVE

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