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Compella — recall 63992

Health Canada — Medical Devices · Canada · 2022-03-14 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 63992
Date of alert: 2022-03-14
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: Physical medicine
Product type: Medical devices

Reported risk: The Compella bed and Compella controllers have power cords included as part of the product. Over the lifespan of each product, the respective power cord from each device can become damaged. Hillrom has received approximately one-hundred ninety-seven (197) complaints, including two (2) reported instances of electrical shock injuries. Recall start date: Feb 25, 2022

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/compella

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Compella — recall 63992

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