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Xhibit telemetry receiver (xtr) 96280 v.1.4.0

Official notice

13 Jun 2022

Last checked

13 Jun 2022

Critical riskHealth Canada

An official Health Canada notice concerns Xhibit telemetry receiver (xtr) 96280 v.1.4.0. An error associated with the operating system causes this defect. After approximately 25 days of continuous use, technical alarm escalation does not occur as specified and expected. All clinical alarms functions as intended and initial technical alarms initiate as intended, but the technical alarm escalation, which occurs after a technical alarm continues for an additional time, does not occur. The fact that this involves technical alarms and not clinical alarm drove the difficulty in more timely recognition of the potential safety risk associated with this defect. The safety concern is based upon the potential that a caregiver may not respond to the initial alarm and is not made aware of the continuing technical failure because of the failure of the secondary (the escalating) alarm. A patient event could occur and without the escalation to indicate a higher severity, the delayed or lack of response from the caregiver could result in injury or death of the patient. In addition, if the alarm acknowledge feature is used, there would be no breakthrough reminder to the caregiver in the form of an alarm escalation. Technical alarms include: 1. All leads off, 2. Low battery, 3. Signal loss, 4. Signal interference, and 5. Spo2 sensor off. As notable from the associated complaints, many customers have detected the issue, but no occurrence have led to any harm. Recall start date: June 2, 2022 Published 2022-06-13.

What to do now

Contact the manufacturer if you require additional information.

Recall number

64262

Official notice

2022-06-13

The hazard

An error associated with the operating system causes this defect. After approximately 25 days of continuous use, technical alarm escalation does not occur as specified and expected. All clinical alarms functions as intended and initial technical alarms initiate as intended, but the technical alarm escalation, which occurs after a technical alarm continues for an additional time, does not occur. The fact that this involves technical alarms and not clinical alarm drove the difficulty in more timely recognition of the potential safety risk associated with this defect. The safety concern is based upon the potential that a caregiver may not respond to the initial alarm and is not made aware of the continuing technical failure because of the failure of the secondary (the escalating) alarm. A patient event could occur and without the escalation to indicate a higher severity, the delayed or lack of response from the caregiver could result in injury or death of the patient. In addition, if the alarm acknowledge feature is used, there would be no breakthrough reminder to the caregiver in the form of an alarm escalation. Technical alarms include: 1. All leads off, 2. Low battery, 3. Signal loss, 4. Signal interference, and 5. Spo2 sensor off. As notable from the associated complaints, many customers have detected the issue, but no occurrence have led to any harm. Recall start date: June 2, 2022

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Recall Numbers

64262

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Affected products

Product 1

Affected products - Xhibit Telemetry Receiver (Xtr) 96280 V.1.4.0, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 96280

Risk / hazard

An error associated with the operating system causes this defect. After approximately 25 days of continuous use, technical alarm escalation does not occur as specified and expected. All clinical alarms functions as intended and initial technical alarms initiate as intended, but the technical alarm escalation, which occurs after a technical alarm continues for an additional time, does not occur. The fact that this involves technical alarms and not clinical alarm drove the difficulty in more timely recognition of the potential safety risk associated with this defect. The safety concern is based upon the potential that a caregiver may not respond to the initial alarm and is not made aware of the continuing technical failure because of the failure of the secondary (the escalating) alarm. A patient event could occur and without the escalation to indicate a higher severity, the delayed or lack of response from the caregiver could result in injury or death of the patient. In addition, if the alarm acknowledge feature is used, there would be no breakthrough reminder to the caregiver in the form of an alarm escalation. Technical alarms include: 1. All leads off, 2. Low battery, 3. Signal loss, 4. Signal interference, and 5. Spo2 sensor off. As notable from the associated complaints, many customers have detected the issue, but no occurrence have led to any harm. Recall start date: June 2, 2022

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Spacelabs Healthcare, Xhibit Telemetry Receiver 96280 V.1.4.0.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

critical

Recall details

Recall number

64262

Classification

Type II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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