FDA·Medical devices·July 1, 2026

Ventec recalls VOCSN+Pro ventilator over damaged backup alarm battery

The ventilator's backup battery for the backup alarm may be damaged, so the alarm might not sound if main power is lost and other backup power is missing or used up, delaying caregivers from noticing a dangerous situation.

What to do

The notice does not give instructions. Read the official notice for details.

Do not stop taking a prescribed medicine, or stop using a device you rely on, until you have talked to your pharmacist or doctor.

Recall details

Product
VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001
Hazard
Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result in the backup alarm not activating during loss of primary power and absence/depletion of backup power sources, which may result in delayed caregiver awareness of a hazardous condition.
Units
1
Where sold
US Nationwide distribution in the state of UT.
FDA classification
Class II · Ongoing
Classified by FDA
June 23, 2026
Recall started
May 8, 2026
FDA enforcement report
July 1, 2026
Identifiers
  • Codes: REF/UDI-DI/Serial Number/Lot: PRT-00853-000/00855573007839/155391P/807138, PRT-00490-001/00855573007792/155391/804613
  • FDA recall number: Z-2525-2026

The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.

Official notice

The notice's own wording from FDA.

Product
VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001
Reason for recall
Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result in the backup alarm not activating during loss of primary power and absence/depletion of backup power sources, which may result in delayed caregiver awareness of a hazardous condition.
Classification
Class II (Ongoing)
Distribution
US Nationwide distribution in the state of UT.
Quantity
1

Related recalls