Covidien recalls TEMP SENSE silicone catheters that may show lower body temperature readings than actual patient temperature. Affected units include specific item codes and serial numbers.
The temperature sensor catheters may be defective in that they will show a lower body temperature measurement than the actual temperature of the patient.
Covidien is recalling TEMP SENSE silicone catheters that may show lower body temperature readings than the actual patient temperature. This could lead to inaccurate medical assessments if used in patient monitoring.
The temperature sensor catheters may provide lower temperature readings than the actual patient temperature. This could lead to incorrect medical decisions if the device is used for patient monitoring. Inaccurate readings might affect treatment decisions.
Healthcare professionals using these catheters for patient temperature monitoring are most at risk. Patients receiving care with these devices may experience inaccurate temperature readings.
Check for the item code 50514T or serial numbers 1733850164 and 1805050064 on the device packaging or label.
Look for the item code 50514T or serial numbers 1733850164 and 1805050064 on the device packaging or label.
The temperature sensor catheters may show lower body temperature measurements than the actual temperature of the patient.
Check for the item code 50514T or serial numbers 1733850164 and 1805050064 on the device packaging or label.
The recall does not specify a remedy, so contact the manufacturer for further instructions.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-3204-2018 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-3204-2018 from Covidien. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
