---
title: "Hillrom Temperature Management Controller, MP, Model # 2083516; used in conju... — FDA record Z-0841-2025 | Is It on Recall"
description: "HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 may experience a Power-on self-test error co"
url: https://isitonrecall.com/recall/fda-device-z-0841-2025-hillrom-temperature-management-controller-mp-model-2083516-used-in-conjunction-with-warming-blankets/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Hillrom Temperature Management Controller, MP, Model # 2083516; used in conjunction with Warming Blankets and Mattres... — FDA record Z-0841-2025

Reported completed

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 Mar 14, 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**: Hillrom Temperature Management Controller, MP, Model # 2083516; used in conjunction with Warming Blankets and Mattresses.
- **Reason**: HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 may experience a Power-on self-test error code "EA POST".
- **Classification**: Class II
- **Recalling firm**: Augustine Temperature Management, LLC
- **Quantity**: 77 units
- **Agency-reported status**: Completed
- **Source record identifier**: Z-0841-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0841-2025%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 00850011479582, Serial Numbers: 23010166, 23010167, 23010168, 23010169, 23010170, 23010171, 23010172, 23010173, 23010174, 23010175, 23010176, 23010177, 23010178, 23010179, 23010180, 23010181, 23010182, 23010183, 23010184, 23010185, 24020001, 24020002, 24020003, 24020004, 24020005, 24020006, 24030001, 24030002, 24030003, 24030004, 24030005, 24030021, 24030022, 24030023, 24030024, 24030025, 24030026, 24030027, 24030028, 24030029, 24030030, 24030016, 24030017, 24030018, 24030019, 24030020, 22120033, 24030011, 24030012, 24030013, 24030014, 24030015, 24030006, 24030007, 24030008, 24030009, 24030010, 24060001, 24060002, 24060003, 24060004, 24060005, 24060006, 24060007, 24060008, 24060009, 24060010, 24060024, 24060025, 24060026, 24060027, 24060028, 24060011, 24060012, 24060013, 24060014, 24060015. |

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

## Distribution

Worldwide

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Jan 22, 2025
- **Recall initiation date**: Mar 14, 2022
- **Center classification date**: Jan 10, 2025

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-0841-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Augustine Temperature Management, LLC records](https://isitonrecall.com/brand/augustine-temperature-management-llc/)