Philips Respironics recalls Trilogy Evo CPAP devices with specific product numbers and software versions due to potential pressure increases affecting infants and children.
Two software issues have been identified related to pressure increase in the device: The first issue is described as "Infant/Pediatric EFS Calibration Pressure Increase" and the second issue is described as "Pressure Drift (Continuous Usage).
Philips Respironics is recalling certain Trilogy Evo CPAP devices because software issues may cause pressure increases, which could be harmful to infants and children. This recall affects specific product numbers and software versions sold in various countries.
Two software issues can cause the device to increase pressure unexpectedly. The first issue affects infant/pediatric EFS calibration, and the second issue causes continuous pressure drift during use. These problems may lead to unsafe pressure levels for users.
Parents and caregivers of infants and children using the recalled Trilogy Evo CPAP devices are most at risk. The recall applies to specific product numbers and software versions sold globally.
Check the product number on your device, which includes codes like BL2110X15B or CA2110X12B. Also, verify the software version number, such as 1.02.01.00 or 1.03.05.00.
Look for the product number on your device, which includes codes like BL2110X15B or CA2110X12B.
Check the software version number on your device, such as 1.02.01.00 or 1.03.05.00.
Philips Respironics identified two software issues that may cause pressure increases in the device, which could be harmful to infants and children.
Software versions 1.02.01.00, 1.03.05.00, 1.03.07.00, 1.04.02.00, 1.04.06, 1.05.01, and 1.06.02 are affected.
Check the product number on your device (e.g., BL2110X15B) and the software version number (e.g., 1.02.01.00).
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-2287-2021 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-2287-2021 from Philips Respironics. 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.
