FDA Device recall Z-1172-2025
Augustine Surgical Inc
- FDA Device
- Class II
- ongoing
- Published 2025-02-26
On 2025-02-26 the FDA classified a Class II recall of Augustine Surgical Inc by Augustine Temperature Management, citing users were experiencing the following error message (M-0B-125) stated Check Neutral Electrode Contact .
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1172-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-02-15 |
| Published | 2025-02-26 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Augustine Temperature Management |
| Distribution | AL, NV, TX |
Product
Augustine Surgical Inc. HotDog Return Electrode accessory connector cables, Model A138 used in conjunction with Warming Blankets and Mattresses.
Reason
Users were experiencing the following error message (M-0B-125) stated Check Neutral Electrode Contact .
Identifiers
| code_info | UDI-DI 00850011479674, Lot Number 2339 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1172-2025%22
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