Physio-Control recalls LIFEPAK 15 defibrillators with specific catalog numbers due to required inspections not being performed after servicing. Affected units may have safety risks if not properly maintained.
Due to required inspections not being performed on products/units that have gone through servicing.
Physio-Control is recalling specific LIFEPAK 15 defibrillators because required inspections were not done after servicing. This could lead to safety issues if the device is used without proper maintenance.
The hazard occurs because required inspections were not performed on the defibrillators after servicing. This means the device might not be safe to use if it has been serviced but not properly checked for safety.
Trained medical personnel who use the LIFEPAK 15 defibrillator in emergency care settings are most at risk if they own or use the recalled units. The recall affects specific model numbers and serial numbers.
Check for the specific catalog numbers and UDI-DI codes listed: V15-7-000022, 99577-001957, 883873871690, V15-2-000051, 99577-000046, 883873988022, and other listed codes. The device is intended for use by trained medical personnel in emergency care settings.
Identify if your LIFEPAK 15 has the specific catalog numbers or UDI-DI codes listed in the recall notice.
The recall is due to required inspections not being performed on products after servicing, which could affect safety.
The official notice does not specify a remedy, so check the recall details to see if your unit is affected and contact Physio-Control for further instructions.
The recall indicates that the device may not be safe if required inspections were not done after servicing, so it's recommended to verify your unit's status.
We’ve drafted a message you can send Physio-Control to request your refund or repair — edit it as you like.
Subject: Recall Z-2497-2025 — Physio-Control Physio-Control Hello, I own a Physio-Control that is covered by recall Z-2497-2025 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.
