---
title: "(1) CareEvent, Model No. 866435 (2) CareEvent Upgrade, Model no. 866436 — FDA record Z-0732-2024 | Is It on Recall"
description: "Push notifications may fail to send to the user under certain conditions. This could potentially result in patient harm due to delay in detection of a change in"
url: https://isitonrecall.com/recall/fda-device-z-0732-2024-1-careevent-model-no-866435-2-careevent-upgrade-model-no-866436/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# (1) CareEvent, Model No. 866435 (2) CareEvent Upgrade, Model no. 866436 — FDA record Z-0732-2024

Reported ongoing

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 Nov 28, 2023. 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**: (1) CareEvent, Model No. 866435 (2) CareEvent Upgrade, Model no. 866436
- **Reason**: Push notifications may fail to send to the user under certain conditions. This could potentially result in patient harm due to delay in detection of a change in patient condition.
- **Classification**: Class II
- **Recalling firm**: Philips North America
- **Quantity**: 254 US; 37 OUS
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0732-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0732-2024%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 | UDI-DI: 00884838099128 Software: CareEvent Version C.03.X |

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

## Distribution

Worldwide distribution: US (Nationwide) to states of: CA, GA, IA, MA, MI, MN, NJ, NM, NY, OH, PA, TN, TX, WA, WV; and OUS (Foreign) distribution to countries of: Australia, Austria, Belarus, Belgium, Brazil, Canada, Czech Republic, Denmark, Estonia, Faroe Islands, Finland, France, Germany, India, Indonesia, Ireland, Italy, Japan, Lithuania, Luxembourg, Mexico, Netherlands, New Zealand, Norway, Oman, Philippines, Poland, Romania, Saudi Arabia, Singapore, Slovakia, South Africa, South Korea, Spain, Sweden, Switzerland, Thailand, United Kingdom, Utd.Arab.Emir., and Uzbekistan

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

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [New Jersey](https://isitonrecall.com/state/new-jersey/)
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- [Nevada](https://isitonrecall.com/state/nevada/)
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- [Ohio](https://isitonrecall.com/state/ohio/)
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- [Oregon](https://isitonrecall.com/state/oregon/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [West Virginia](https://isitonrecall.com/state/west-virginia/)
- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jan 24, 2024
- **Recall initiation date**: Nov 28, 2023
- **Center classification date**: Jan 13, 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-0732-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Philips North America records](https://isitonrecall.com/brand/philips-north-america/)
