HomeMedical Device recalls
Medium severity

BARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER

SourceFDA Device Enforcement
CategoryMedical Device
SeverityMedium
Statusongoing
Recall dateApril 10, 2026
ReportedMay 20, 2026
Recalling firmStryker Sustainability Solutions
Country / regionUnited States AZ

Hazard

Incomplete seals on sterile product

Affected products

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