Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Open, Classified

Augustine Surgical Inc. HotDog Return Electrode accessory connector cables, Model A136 used in conjunction with Warming Blankets and Mattresses.

FDA Recall Z-1171-2025 · Posted 2025-02-14

Recalling FirmAugustine Temperature Management, LLC
Recall StatusOpen, Classified
Product CodeDWJ
Date Initiated2024-02-15
Product Quantity20 units

Reason for Recall

Users were experiencing the following error message (M-0B-125) stated Check Neutral Electrode Contact .

Firm Action

Augustine Temperature Management contacted their consignees by visit beginning on 02/15/2024 to replace the affected cables. The firm collected email confirmation that the original cables had either been returned or destroyed. If you have any questions, contact the Product Manager at 952-465-3526 or email:

Root Cause

Device Design

Distribution Pattern

US distribution to states of: AL, TX, NV

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K230866HotDog Warming Mattress + Return ElectrodeAugustine Temperature Management, LLC · 2023-06-29K210727HotDog Warming Mattress + Return ElectrodeAugustine Temperature Management, LLC · 2022-02-01

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑