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Source: FDA | Recall date: 05/20/2026
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Affected product: BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER
Summary: Incomplete seals on sterile product
Hazard: Incomplete seals on sterile product
Track your baby products and get automatic recall alerts when something may affect your family.
Learn more about the baby product recall tracker, baby product recall alerts, or recall monitoring plans.