# Major Recall Alert: LIFEPAK 35 Monitor/Defibrillator Recalled Due to Handle Detachment Issues
On *August 15, 2025*, a major recall was issued for the *LIFEPAK 35 Monitor/Defibrillator*, a critical medical device manufactured by Stryker. Reports indicate that the device's handles have been detaching unexpectedly, posing potential safety risks during patient care. Healthcare professionals and organizations relying on these devices should take immediate action to address the recall and ensure safety.
Learn more about the details of this recall, why it matters, and steps you should take to remain compliant and informed.
## Why This Recall Is Important
The *LIFEPAK 35 Monitor/Defibrillator* is widely used in medical emergencies to monitor patients and deliver life-saving defibrillation when cardiac arrest occurs. As these devices are integral to healthcare settings, any malfunctions can have serious repercussions for patient safety.
The reported issue involves handles detaching from the device, potentially causing mishandling during critical patient care. This could delay treatment or damage the device, putting patient lives at risk.
### Key Risks Associated with the Recall:
- **Device malfunctions:** Detached handles may disrupt emergency responses.
- **Potential injuries to personnel:** If the device is dropped due to a detached handle, personnel could be injured.
- **Equipment damage:** Damaged packs may lead to delays in care and expensive replacements.
Given its crucial role, this recall highlights the importance of ensuring all medical devices meet the highest safety standards.
## Details of the Recall
The following details outline the critical information surrounding this recall:
- **Product Name:** LIFEPAK 35 Monitor/Defibrillator
- **Brand Name:** LIFEPAK
- **Manufacturer:** Stryker
- **Issue:** Detached handles from the monitor/defibrillator
- **Recall Start Date:** August 15, 2025
- **Reason for Recall:** Multiple reports of the critical device handles detaching during use, creating potential safety hazards.
Stryker is actively addressing these concerns. Healthcare professionals and institutions that use this device should remain vigilant and adhere to instructions issued by Stryker to avoid adverse incidents.
For more information, review the official recall notice issued by the Canadian government: [LIFEPAK 35 Monitor/Defibrillator Recall Notification](https://recalls-rappels.canada.ca/en/alert-recall/lifepak-35-monitordefibrillator).
## What You Should Do
If you or your healthcare organization uses the *LIFEPAK 35 Monitor/Defibrillator*, here are the recommended steps to take:
- **Immediately inspect your devices:** Check all LIFEPAK 35 units under your care for potential damage or detached handles.
- **Contact Stryker for guidance:** If you identify any issues, reach out to Stryker’s customer support team for recommendations and solutions.
- **Follow recall instructions:** Adhere to any notifications sent by Stryker or health authorities about device repairs, replacements, or disposal.
- **Keep detailed records:** Document the serial numbers and condition of all recalled devices for future follow-up.
- **Ensure alternative availability:** Equip your facility with backup medical devices to ensure uninterrupted care during the recall process.
Acting swiftly and responsibly is essential to safeguard patient care and minimize disruptions.
## Stay Safe – Get Instant Recall Alerts
Medical device recalls can have far-reaching impacts. Stay informed by signing up for recall alerts to receive updates as soon as they’re announced. Keeping track of these notifications ensures that healthcare facilities can respond proactively and maintain the highest safety standards.
**Download our free Recall App today** to get real-time alerts directly to your smartphone. Stay ahead of urgent safety notifications for medical devices like the *LIFEPAK 35 Monitor/Defibrillator* and other essential products.
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Your vigilance can make a difference in protecting the lives of patients and ensuring the continued integrity of your healthcare operations. For additional details, visit the official recall page [here](https://recalls-rappels.canada.ca/en/alert-recall/lifepak-35-monitordefibrillator).