← FDA ENFORCEMENT
Z-1637-2026Class I

Baxter Healthcare Corporation

Recalling firm
Baxter Healthcare Corporation
Product type
Device
Status
Ongoing
Report date
2026-04-08
Distribution
Florida
Firm state
IL
Product quantity
19 units
Initiated by
Voluntary: Firm initiated
Reason for recall

Urgent Medical Device Correction for the Volara system single-patient use circuit due to the potential that patients or caregivers may be unaware of a possible decrease in oxygen levels (oxygen desaturation), or potential lung tissue injury from overexpansion (barotrauma) when the Volara device is used in the home care environment. This correction is providing the home caregiver specific instructions for use.

Product description

Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxter Volara Respiratory Therapy system.

Code / lot info

UDI/DI number 00887761984622

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.