---
title: "Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044 — FDA record Z-2272-2026 | Is It on Recall"
description: "Temperature probe devices lack FDA clearance."
url: https://isitonrecall.com/recall/fda-device-z-2272-2026-covidien-mon-a-therm-general-purpose-temperature-probe-ref-90044/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044 — FDA record Z-2272-2026

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 Apr 23, 2026. 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**: Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
- **Reason**: Temperature probe devices lack FDA clearance.
- **Classification**: Class II
- **Recalling firm**: Covidien LLC
- **Quantity**: 1775 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2272-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2272-2026%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: 30884521828388/ Lot: 25F0945JZX 25H0949JZX, 25I1065JZX, 25I1066JZX |

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

## Distribution

US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, FL, GA, HI, IL, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, WA, WV.

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/)
- [Alabama](https://isitonrecall.com/state/alabama/)
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- [Nevada](https://isitonrecall.com/state/nevada/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Ohio](https://isitonrecall.com/state/ohio/)
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- [Oregon](https://isitonrecall.com/state/oregon/)
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- [Rhode Island](https://isitonrecall.com/state/rhode-island/)
- [South Carolina](https://isitonrecall.com/state/south-carolina/)
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- [Texas](https://isitonrecall.com/state/texas/)
- [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**: Jun 10, 2026
- **Recall initiation date**: Apr 23, 2026
- **Center classification date**: May 29, 2026

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-2272-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Covidien Llc records](https://isitonrecall.com/brand/covidien-llc/)