---
title: "Augustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Contr... — FDA record Z-0701-2025 | Is It on Recall"
description: "Instructions for use update on HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 pertaining to"
url: https://isitonrecall.com/recall/fda-device-z-0701-2025-augustine-surgical-inc-hot-dog-patient-warming-temperature-management-controller-multiport-models-1/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Augustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Multiport, Models: 1) Model # WC7... — FDA record Z-0701-2025

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 Dec 4, 2024. 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**: Augustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Multiport, Models: 1) Model # WC77, 2) Model # WC77D (Demo), 3) Model # WC77R (Refurbished); used in conjunction with Warming Blankets and Mattresses.
- **Reason**: Instructions for use update on HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 pertaining to Power-on self-test error code "EA POST".
- **Classification**: Class II
- **Recalling firm**: Augustine Temperature Management, LLC
- **Quantity**: 1776 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0701-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0701-2025%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 | 1) UDI-DI 00850011479025, Serial Numbers: 20080060-24060065; 2) UDI/DI 00850011479292, Serial Numbers: 20080060-24060065; 3) UDI-DI 00850011479308, Serial Numbers: 20080060-24060065 |

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

## Distribution

US and Canada

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

## Dates in the source

- **Report date**: Dec 25, 2024
- **Recall initiation date**: Dec 4, 2024
- **Center classification date**: Dec 18, 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-0701-2025%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/)