Baxter Healthcare Corporation Hillrom VOLARA P.CIRCUIT 5KIT (System Single Patient Use Circuit), Model/Catalog Number REF M08270

Source: FDA | Recall date: 05/21/2026

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Affected product: Hillrom VOLARA P.CIRCUIT 5KIT (System Single Patient Use Circuit), Model/Catalog Number REF M08270

Brand: baxter healthcare corporation

Hazard: There have been reports of air and medication leakage f⁠rom the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment.

Official identifiers

FDA recall number: Z-2549-2026
FDA event number: 99119

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