Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401905; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Recall date
- April 10, 2026
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2192-2026
- FDA classification
- Class II
- Brand / firm
- Stryker Sustainability Solutions
- Sold / distributed
- US Nationwide and the countries of Israel and Canada.
Why it was recalled
Incomplete seals on sterile product
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Daig Livewire Steerable, Product Number 401905; REPROCESSED ELECTROPHYSIOLOGY CATHETER
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