Ventec Life Systems (PRT-01098-100) Recall
VC(Japan) Model Number: PRT-01098-100, Package PN:PRT-01125-100. used for ventilatory support.
What is the FDA recall status?
The FDA record lists this recall as ongoing. FDA enforcement data is not a live recall-lifecycle tracker. Follow the official instructions and check the agency notice or firm for current guidance.
Why was Ventec Life Systems recalled?
Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.
What should I do if I have this product?
Follow the firm and FDA instructions for the affected product. Contact the recalling firm for current guidance.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare your product with the product description and available lot, UPC or model codes below from the official FDA record to check whether it is covered by this recall. If an identifier is missing or unclear, check the complete official notice or contact the firm; an incomplete match here does not establish that your product is unaffected.
Full product description
VC(Japan) Model Number: PRT-01098-100, Package PN:PRT-01125-100. used for ventilatory support.
Which lot codes, UPCs or models are affected?
All Serial Numbers: UDI: 00850018761116
- Agency record number
- Z-0131-2027
- Product
- VC(Japan) Model Number: PRT-01098-100, Package PN:PRT-01125-100. used for ventilatory support.
- Recalling firm
- Ventec Life Systems, Inc.
- Quantity
- 180 units
- Distribution
- Distribution US nationwide including Puerto Rico.
- Recall started
- September 17, 2026
- Report date
- October 28, 2026
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)