---
title: "Philips OmniWire Pressure guide wire REF 89185J PN 300000252891 — FDA record Z-1270-2022 | Is It on Recall"
description: "Due to a potential failed sterilization process."
url: https://isitonrecall.com/recall/fda-device-z-1270-2022-philips-omniwire-pressure-guide-wire-ref-89185j-pn-300000252891/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Philips OmniWire Pressure guide wire REF 89185J PN 300000252891 — FDA record Z-1270-2022

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 16, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Philips OmniWire Pressure guide wire REF 89185J PN 300000252891
- **Reason**: Due to a potential failed sterilization process.
- **Classification**: Class II
- **Recalling firm**: Volcano Corp
- **Quantity**: 11 devices
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-1270-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1270-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Model Number: 89185J Part Number: 300000252891 UDI Code: (01)00845225003050(11)220309(17)250309(10)0302535768 Serial Numbers: 37583 37586 37590 37598 37612 37648 37655 37692 37694 37709 37719 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

U.S.: WA and WI O.U.S.: Canada

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Washington](https://isitonrecall.com/state/washington/)
- [Wisconsin](https://isitonrecall.com/state/wisconsin/)

## Dates in the source

- **Report date**: Jun 22, 2022
- **Recall initiation date**: May 16, 2022
- **Center classification date**: Jun 16, 2022
- **Termination date**: Dec 23, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1270-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Volcano Corp records](https://isitonrecall.com/brand/volcano-corp/)