Augustine recalls specific models of patient warming controllers due to potential power-on self-test error code EA POST. Affected units include WC77, WC77D, and WC77R with serial numbers starting 20080060-24060065.
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".
Augustine is recalling certain patient warming controllers that may display a power-on self-test error code 'EA POST'. This could indicate a malfunction that might affect patient safety during medical procedures.
The error code 'EA POST' may indicate a problem with the device's power-on self-test process. This could lead to improper temperature management for patients during medical procedures if the device fails to function correctly.
Healthcare providers using the specific models of patient warming controllers listed in the recall. Patients are at risk if the device malfunctions during medical procedures.
Check for model numbers WC77, WC77D (demo), or WC77R (refurbished) on the device. Serial numbers start with 20080060-24060065. These units are used with warming blankets and mattresses in medical settings.
Identify the model number on the device to see if it is WC77, WC77D, or WC77R.
Check the serial number, which starts with 20080060-24060065, to confirm if the device is affected.
The recall is for devices that display a power-on self-test error code 'EA POST'.
Models WC77, WC77D (demo), and WC77R (refurbished) with serial numbers starting 20080060-24060065.
The recall indicates a potential malfunction, but the remedy is not specified, so there is no immediate stop-use instruction.
We’ve drafted a message you can send Augustine to request your refund or repair — edit it as you like.
Subject: Recall Z-0701-2025 — Augustine Augustine Hello, I own a Augustine that is covered by recall Z-0701-2025 from Augustine. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
