Physio-Control LIFEPAK 15 Defibrillator: Battery Pin Loose Risk

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Recalling firmPhysio-Control, Inc.11811 Willows Rd Ne, N/A · Redmond, WA 98052-2003

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Physio-Control is recalling LIFEPAK 15 defibrillators that may have loose battery pins causing power issues. This could lead to the device not working properly during emergencies.

Why it’s dangerous

Loose battery pins can cause power issues in the defibrillator, potentially leading to the device failing during critical cardiac emergencies. This is a technical issue that may not cause immediate harm but could affect device reliability.

Who’s affected

Healthcare professionals using LIFEPAK 15 defibrillators for emergency cardiac care are most at risk. The recall affects specific units with the serial number 49618486 and part number V15-7-000002.

How to tell if you have this one

Check the serial number on the device (49618486) and part number (V15-7-000002). The recall applies to LIFEPAK 15 defibrillators sold with these specific identifiers.

Brand
Physio-Control
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Serial Number
Look for the serial number 49618486 on the device to confirm if it is affected.

✎ GovInfoNow

Questions people ask

Is this recall dangerous?

The recall indicates a potential for power issues due to loose battery pins, but it does not specify a risk of serious injury. The hazard level is low risk.

How can I tell if my LIFEPAK 15 is affected?

Check the serial number (49618486) and part number (V15-7-000002) on your device to confirm if it is affected.

What should I do if my device is affected?

The recall does not provide a remedy, so contact Physio-Control directly for further instructions.

Take action

Contact Physio-Control

We’ve drafted a message you can send Physio-Control to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0300-2024 — Physio-Control Physio-Control

Hello,

I own a Physio-Control that is covered by recall Z-0300-2024 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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Where this comes from

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.

Official source: FDA Recall #Z-0300-2024 (September 29, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0300-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Physio-Control, Inc. recalls LIFEPAK 15, REF: 99577-001373, Part Number V15-7-000002

Lower-risk recall