# Major Recall Alert: LNCS-II Rainbow DCI 8 SpCO, LNCS-II Rainbow DCIP 8 SpCO, and RD Rainbow SpCO Sensors Recalled Due to LIFEPAK 15 V4 Error
Stryker has issued an important recall affecting the LNCS-II Rainbow DCI 8 SpCO, LNCS-II Rainbow DCIP 8 SpCO, and RD Rainbow SpCO sensors. The issue involves complaints that the LIFEPAK 15 V4 monitor displays an error message, “SpO2: Sensor does not support SpCO or SpMET.” This malfunction prevents users from utilizing the vital SpCO (carbon monoxide) and SpMet (methemoglobin) monitoring functionalities when these devices connect to specific lots of Masimo Rainbow Sensors. Some of these affected sensor lots are also compatible with the LIFEPAK 15 V1 and V2 devices.
Healthcare professionals and facilities utilizing these products should take this recall seriously, as it could lead to interruptions in obtaining critical patient data.
## Why This Recall is Important
The recall centers around a serious technical issue that interferes with the functionality of LIFEPAK 15 V4 units—devices designed for life-saving patient monitoring. When these units are connected to particular Masimo Rainbow Sensor lots, the error message disables SpCO and SpMet readings. These measurements are crucial for diagnosing and managing carbon monoxide poisoning and methemoglobinemia.
Failure to detect or monitor harmful levels of carbon monoxide or methemoglobin can result in delayed treatment, potentially putting patient lives at risk. Ensuring the accuracy and reliability of medical equipment, especially those used in emergency settings, is critical for optimal patient care outcomes.
## Details of the Recall
Below are the key details to help users identify if they are affected by this recall:
- **Category**: Medical Monitoring Equipment
- **Impacted Devices**: LNCS-II Rainbow DCI 8 SpCO, LNCS-II Rainbow DCIP 8 SpCO, RD Rainbow SpCO sensors
- **Affected Device Compatibility**: LIFEPAK 15 V4 models (error-specific issues) and some specific sensor lots compatible with LIFEPAK 15 V1 and V2 models
- **Issue Identified**: Error message – “SpO2: Sensor does not support SpCO or SpMET” prevents SpCO and SpMet usage
- **Reported Complaints**: Multiple complaints submitted to Stryker
- **Announcement Date**: [Insert Correct Recall Date]
For additional details, visit the official Canadian recall notice here: [LIFEPAK 15 V4 Recall – Recalls and Safety Alerts](https://recalls-rappels.canada.ca/en/alert-recall/lifepak-15-v4-spcospmet-sensors).
## What You Should Do
If you currently use these sensors or are responsible for medical monitoring devices in your facility, follow these steps immediately:
- **Check Your Equipment**: Verify if your LIFEPAK 15 V4 or compatible devices are connected to the affected Masimo Rainbow sensors (LNCS-II Rainbow DCI 8 SpCO, LNCS-II Rainbow DCIP 8 SpCO, or RD Rainbow SpCO).
- **Inspect Error Messages**: Look for the error message, "SpO2: Sensor does not support SpCO or SpMET," when connected to affected sensors.
- **Stop Using Affected Sensors**: For patient safety, discontinue the use of impacted sensors and replace them with unaffected equipment.
- **Contact Stryker**: Reach out to Stryker for guidance on replacement options, troubleshooting, or additional recall instructions.
Prompt action is crucial to ensure that patient monitoring systems continue to function as intended without interruptions.
## Stay Safe – Get Instant Recall Alerts
Recalls like these underscore the importance of staying informed. Faulty medical devices can cost valuable time in emergency scenarios. To ensure you never miss critical product recalls, download the MyRecalls app today. With real-time updates, notifications, and safety information at your fingertips, you can act quickly to safeguard your patients, family, and organization from risks.
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Stay informed and act fast to ensure safety in every situation. For additional information or updates, visit [Canada Recalls & Safety Alerts](https://recalls-rappels.canada.ca/en/alert-recall/lifepak-15-v4-spcospmet-sensors).