Augustine Temperature Management recalls 82cm warming mattresses with US501 model to prevent overheating after 1 year of use due to cable connector issues.
There is over-molding that stabilizes the connection between the cable and cable-entry on the mattress. It turns out that after about a year of use, the connector cable on the mattress can experience the same type of deflection that caused the intermittent connection with the cables connecting to the ESU.
Augustine Temperature Management recalls specific warming mattresses to prevent overheating risks after about a year of use. The over-molding in the cable connector can cause intermittent connections that may lead to overheating.
The over-molding in the cable connector can cause the connector to deflect after about a year of use. This may lead to intermittent connections that could cause overheating in the patient.
Patients using this warming mattress for hypothermia treatment. Those with the specific model and serial numbers are most at risk.
Check for the model number US501 and serial numbers 1304292, 1304293, 1304296, or 1304297 on the mattress. The product is an 82 cm (32") underbody warming mattress.
Verify the model number and serial numbers to confirm if your mattress is affected.
The over-molding in the cable connector can cause the connector to deflect after about a year of use, potentially leading to intermittent connections and overheating risks.
The recall record does not specify a remedy, so contact the manufacturer for further instructions.
Check for the model number US501 and serial numbers 1304292, 1304293, 1304296, or 1304297 on the mattress.
We’ve drafted a message you can send Augustine Temperature Management to request your refund or repair — edit it as you like.
Subject: Recall Z-1197-2025 — Augustine Temperature Management Augustine Temperature Management Hello, I own a Augustine Temperature Management that is covered by recall Z-1197-2025 from Augustine Temperature Management. 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.