[FDAPulse](/v/fdapulse) / compare

# Class I recall Z-0123-2027: Ventec Life Systems, Inc. vs Class I recall Z-0152-2027: Philips Ultrasound, LLC: FDAPulse comparison

**Class I recall Z-0123-2027: Ventec Life Systems, Inc. (2026-10-28) and Class I recall Z-0152-2027: Philips Ultrasound, LLC (2026-10-28) are peer FDAPulse records in Washington.**

Data as of 2026-11-04 · [Compiled by Zalwin](/research/fdapulse) from U.S. FDA openFDA (510(k) clearances and device enforcement reports) Copy citation

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## How does Class I recall Z-0123-2027: Ventec Life Systems, Inc. compare to Class I recall Z-0152-2027: Philips Ultrasound, LLC?

| Field | Class I recall Z-0123-2027: Ventec Life Systems, Inc. | Class I recall Z-0152-2027: Philips Ultrasound, LLC |
|---|---|---|
| Record | Device recall | Device recall |
| Recall number | Z-0123-2027 | Z-0152-2027 |
| Recalling firm | Ventec Life Systems, Inc. | Philips Ultrasound, LLC |
| Classification | Class I | Class I |
| Status | Ongoing | Ongoing |
| Voluntary / mandated | Voluntary: Firm initiated | Voluntary: Firm initiated |
| Specialty | Other | Other |
| Product | VOCSN+Pro (Japan), Model Number: PRT-00490-100, Package PN:PRT-00853-100. used for ventilatory support. | Philips Lumify Diagnostic Ultrasound System |
| Reason | Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy. | Ultrasound system may: 1) Not recognize previous transducer registration, prevent scanning, require re-registration with Wi-Fi/cellular access, which may be unavailable outside of the hospital (ambulances/aircraft/field); 2) At connection between transducer USB cable to tablet/phone, there may be an unstable connection/may disconnect disrupting function. May cause diagnosis/treatment delay. |
| Quantity | 325 units | 13,206 |
| Distribution | Distribution US nationwide including Puerto Rico. | Worldwide - US Nationwide distribution including in the states of CA, MA, IL, NY, OR, GA, TX, WA, FL, PA, WI, LA, NJ, KY, VA, MS, AZ, SC, CT, MN, UT, OH, AL, MI, NH, MO, TN, IN, DC, NE, NM, MT, NV, NC, MD, IA, SD, VT, KS, AK, CO, ID, OK, WV, AR, RI, ME, WY, HI, DE, ND and the countries of CA, NO, HR |
| Recall initiated | 2026-09-17 | 2026-09-24 |
| Reported | 2026-10-28 | 2026-10-28 |
| Firm location | Bothell, WA, United States | Bothell, WA, United States |
| Predicate Speed & CAPA Advisory Opportunity Score | 82/100 | 82/100 |
| Peer rank and all 500 records (CSV) | Every comparable record ranked, with amounts, dates and scores 🔒 Click to unlock → |
| Official source URLs for every peer record | Direct links to each record at its government source 🔒 Click to unlock → |

Official records: [Class I recall Z-0123-2027: Ventec Life Systems, Inc.](https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0123-2027%22) · [Class I recall Z-0152-2027: Philips Ultrasound, LLC](https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0152-2027%22)

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Data from the FDA openFDA API, which may lag official FDA databases. Informational only; not regulatory or legal advice.

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