medical MODERATE Updated 2026-05-20

Stryker Sustainability Solutions recalls Daig Livewire Steerable BDB, Product Number 401918, REPROCES

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Recalled Product

Daig Livewire Steerable BDB, Product Number 401918, REPROCESSED ELECTROPHYSIOLOGY CATHETER

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Hazard / Issue

Incomplete seals on sterile product

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI 00885825007324, Lot Numbers: 4101996, 4175347.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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Search Amazon for Daig Livewire Steerable BDB, →

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