Physio-Control recalls AC power adapters for LIFEPAK 15 defibrillators that may not charge batteries or power on when plugged in. Affected units were made between November 2021 and April 2023.
AC Power Adapter (ACPA) may not charge the monitor/defibrillator batteries and may not allow the monitor/defibrillator to power on while plugged into the ACPA.
Physio-Control is recalling AC power adapters for their LIFEPAK 15 defibrillators because these adapters may not charge the device's batteries or allow it to power on when plugged in. This could prevent the defibrillator from working properly during emergencies.
The AC power adapter may not charge the defibrillator's batteries or power on when plugged in, which could prevent the device from functioning during emergencies. This is a potential issue for healthcare providers using the device in critical situations.
Healthcare professionals using the LIFEPAK 15 defibrillator are most at risk, as the device is critical for emergency cardiac care. Patients using the defibrillator in emergencies could be affected if the adapter fails.
Check for the model reference 11140-000098 on the adapter. The adapters were manufactured between November 3, 2021, and April 24, 2023.
Look for the model reference 11140-000098 on the adapter to confirm if it's affected.
The adapter may not charge the defibrillator batteries or power on when plugged in, which could prevent the device from working during emergencies.
The recall record does not specify a remedy, so no action is required beyond checking if the adapter matches the model reference.
Adapters were manufactured between November 3, 2021, and April 24, 2023.
We’ve drafted a message you can send Physio-Control to request your refund or repair — edit it as you like.
Subject: Recall Z-0567-2024 — Physio-Control Physio-Control Hello, I own a Physio-Control that is covered by recall Z-0567-2024 from Physio-Control. 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.
