Physio-Control recalls LIFEPAK 1000 defibrillators with specific catalog numbers due to required inspections not being performed after servicing. Affected units may pose risks if not properly maintained.
Due to required inspections not being performed on products/units that have gone through servicing.
Physio-Control is recalling certain LIFEPAK 1000 defibrillators because required inspections were not done after servicing. This could lead to improper function if the device is used without proper maintenance.
The hazard occurs because required inspections after servicing were not performed on the defibrillator. This could result in the device not functioning correctly if used without proper maintenance, but it does not indicate an immediate risk during normal use.
Healthcare professionals who use the LIFEPAK 1000 defibrillator for emergency cardiac care are most at risk if the device has not been properly inspected after servicing.
Check for the catalog numbers: 320371500023, 320371500229, or 331706400001 with the serial numbers 99425-000025 and 885074698953.
Look for the catalog numbers 320371500023, 320371500229, or 331706400001 on the defibrillator.
The recall is due to required inspections not being performed on products after servicing, which could lead to improper function if the device is used without proper maintenance.
The official recall notice does not specify a remedy or action steps for affected units.
The recall indicates that the device may not function correctly if not properly maintained, but it does not indicate an immediate risk during normal use.
We’ve drafted a message you can send Physio-Control to request your refund or repair — edit it as you like.
Subject: Recall Z-2498-2025 — Physio-Control Physio-Control Hello, I own a Physio-Control that is covered by recall Z-2498-2025 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.
