Warning
Stryker Sustainability Solutions Recalls Daig Livewire Steerable
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #Z-2196-2026Medical Device
Stryker Sustainability Solutions Recalls Daig Livewire Steerable
Stryker Sustainability Solutions · Class II — Moderate Risk
Product Description
Daig Livewire Steerable, Product Number 401923; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Reason for Recall
Incomplete seals on sterile product
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
US Nationwide and the countries of Israel and Canada.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
Sources: FDA openFDA Enforcement Database