---
title: "Medichoice Infant Heel Warmer, Reference # 989805643721 1079906 — FDA record Z-0509-2022 | Is It on Recall"
description: "After the device was cleared by the FDA, Philips made changes to the labeling that do not fall within the existing FDA clearance. These devices with the modifie"
url: https://isitonrecall.com/recall/fda-device-z-0509-2022-medichoice-infant-heel-warmer-reference-989805643721-1079906/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Medichoice Infant Heel Warmer, Reference # 989805643721 1079906 — FDA record Z-0509-2022

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 29, 2021. 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**: Medichoice Infant Heel Warmer, Reference # 989805643721 1079906
- **Reason**: After the device was cleared by the FDA, Philips made changes to the labeling that do not fall within the existing FDA clearance. These devices with the modified labeling cannot be distributed or sold without new 510(k) clearance.
- **Classification**: Class II
- **Recalling firm**: Philips North America Llc
- **Quantity**: 2,925,800 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0509-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0509-2022%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 | All units are impacted |

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

## Distribution

US Nationwide and Canada.

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

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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jan 26, 2022
- **Recall initiation date**: Nov 29, 2021
- **Center classification date**: Jan 19, 2022

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-0509-2022%22)

## Related records

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