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Source: FDA | Recall date: 05/27/2026
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Affected product: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913
Summary: Certain lots of product have the potential for a sterile barrier breach.
Hazard: Certain lots of product have the potential for a sterile barrier breach.
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.