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Ventec VOCSN+Pro Respiratory System
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MEDICAL DEVICE RECALLMODERATE

Ventec VOCSN+Pro Respiratory System

Ventec is recalling the VOCSN+Pro respiratory system because a damaged battery may prevent the backup alarm from sounding during power loss.

What to do

Contact Ventec Life Systems to arrange for a technician to inspect and replace the affected back-up battery. Continue to monitor the device closely and ensure alternative power sources are available.

Recalled
Listed
Updated
Recall No.
Z-2525-2026
Agency
FDA
Firm
Ventec Life Systems, Inc.
Recall ID
98888
Status
ONGOING

Why it was recalled

Ventec Life Systems is recalling the VOCSN+Pro respiratory system due to a damaged back-up battery. This defect may prevent the backup alarm from activating during a loss of primary power, potentially delaying caregiver awareness of a hazardous condition.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001

Lot code
PRT-00853-000, 155391P, 807138, PRT-00490-001, 155391, 804613
UDI-DI
00855573007839, 00855573007792

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Other Device Defect recalls

Other recent recalls from Ventec Life Systems, Inc.

All recalls from Ventec Life Systems, Inc.

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Editorial summary by Recall Canary · summary updated 2026-06-24 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification