Baxter Healthcare Corporation: Medical Device Recall in 2024 - (Recall #: Z-2322-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Volara System. Blue Ventilator Adapter Module. Intermittent positive pressure breathing device component.

Product Classification:

Class I

Date Initiated: May 30, 2024

Date Posted: July 24, 2024

Recall Number: Z-2322-2024

Event ID: 94713

Reason for Recall:

Potential of the handset plug to disconnect from the nebulizer port on the blue ventilator adapter. The handset plug is required to ensure proper operation and ventilator gas flow.

Status: Ongoing

Product Quantity: 350 units

Code Information:

Product Code: M07937; Lot numbers: 4210495, 4325617.

Distribution Pattern:

Nationwide distribution. International distribution to Canada, France, and Germany.

Voluntary or Mandated:

Voluntary: Firm initiated