Augustine recalls 50" patient warming mattresses with US502 model to prevent intermittent connections due to over-molding after one year of use.
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 a specific patient warming mattress model to prevent intermittent electrical connections that could cause treatment failure. This affects medical devices used for hypothermia treatment.
Over-molding in the connector cable can cause the same deflection that leads to intermittent electrical connections after about a year of use. This may result in treatment failure if the device stops working during patient care.
Healthcare providers using this mattress for patient hypothermia treatment are most at risk. The recall applies to specific models sold with serial numbers starting with 1304283.
Look for the model number US502 on the mattress, which is 50 inches long. The serial numbers start with 1304283 and are labeled on the device.
Look for serial numbers starting with 1304283 on the mattress.
Reach out to Augustine Temperature Management for further assistance with the recall.
The model number is US502, a 50-inch patient warming mattress.
The over-molding issue can cause intermittent connections after about a year of use.
Check the serial number starting with 1304283 and contact Augustine Temperature Management for assistance.
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-1198-2025 — Augustine Temperature Management Augustine Temperature Management Hello, I own a Augustine Temperature Management that is covered by recall Z-1198-2025 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.
