Ventec Life Systems recalls VOCSN, V+ Pro Emergency, VC and VCSN+Pro ventilators over a cable that can disconnect
The internal flow transducer cable connector in these ventilators may disconnect from the internal board, which could make the system reboot and interrupt ventilation therapy.
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 (Japan) Model Number: PRT-01100-100, Package PN:PRT-01126-100. used for ventilatory support.; V+ Pro Emergency, Model Number: PRT-01201-000, Package PN:PRT-01173-000,PRT-01222-000. used for ventilatory support.; VC(Japan) Model Number: PRT-01098-100, Package PN:PRT-01125-100. used for ventilatory support.
- Company
- Ventec Life Systems, Inc.
- Hazard
- Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.
- Units
- 100 units; 30,120 units; 180 units
- Where sold
- Distribution US nationwide including Puerto Rico.
- FDA classification
- Class I · Ongoing
- Classified by FDA
- October 20, 2026
- Recall started
- September 17, 2026
- FDA enforcement report
- October 28, 2026
- Identifiers
- Codes: All Serial Numbers: UDI: 00850018761130
- FDA recall number: Z-0127-2027
- Codes: All Serial Numbers: UDI: 00855573007945
- FDA recall number: Z-0132-2027
- Codes: All Serial Numbers: UDI: 00850018761116
- FDA recall number: Z-0131-2027
- Codes: All Serial Numbers: UDI: 00855573007860
- FDA recall number: Z-0128-2027
- Codes: All Serial Numbers: UDI: 00855573007747
- FDA recall number: Z-0126-2027
- Codes: All Serial Numbers: UDI: 00855573007761, 00855573007204
- FDA recall number: Z-0123-2027
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 (Japan) Model Number: PRT-01100-100, Package PN:PRT-01126-100. used for ventilatory support. | V+ Pro Emergency, Model Number: PRT-01201-000, Package PN:PRT-01173-000,PRT-01222-000. used for ventilatory support. | VC(Japan) Model Number: PRT-01098-100, Package PN:PRT-01125-100. used for ventilatory support. | VCSN+Pro Model Number: PRT-01184-000, Package PN:PRT-01172-000. used for ventilatory support.
- Reason for recall
- Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.
- Classification
- Class I (Ongoing)
- Distribution
- Distribution US nationwide including Puerto Rico.
- Quantity
- 100 units; 30,120 units; 180 units; 4,368 units; 1,532 units; 325 units
Related recalls
Ventec recalls HomeFill oxygen cylinders over missing required medical gas labeling
The HomeFill oxygen cylinders do not carry the medical gas labeling that is required, so users may not have the label information meant to go with the oxygen.
Ventec Life Systems, Inc. · 48 units
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.
Ventec Life Systems, Inc. · 1 unit
Ventec recalls VOCSN V+Pro ventilators over possible oxygen leak that could cause low oxygen delivery and fire risk
Production testing may not have covered all high-pressure conditions, so an oxygen leak could occur, giving patients less oxygen than intended and making fire more likely in the oxygen-enriched air.
Ventec Life Systems, Inc. · 42 units
CooperVision recalls Softmed Breathables Advanced Toric contact lenses over wrong extended wear label on carton
The cartons wrongly say the lenses are "Indicated for Extended Wear", but they are meant for daily wear and the FDA has not approved them for extended wear use.
CooperVision, Inc. · 230856 units
Medtronic MiniMed recalls MiniMed Go app version 1.2.1 because the long-acting dose reminder can stop working
After updating to version 1.2.1, users who had turned on the long-acting dose reminder in version 1.2.0 or earlier may get no reminder, which could lead to missed or delayed insulin doses and high glucose, or double dosing and low glucose.
Medtronic MiniMed, Inc. · 623 units
Integrated Medcraft recalls FORWARD Gunshot Wound Kit because its sterile pad can break down
Internal testing found the kit's sterile pad may degrade over time, and bits of the nonwoven pad material may come loose on the wound or close to the wound.
Integrated Medcraft LLC · 1033 units