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Enterprise 9000x with indigo module
Official notice
8 Sept 2023
Last checked
8 Sept 2023
An official Health Canada notice concerns Enterprise 9000x with indigo module. Arjo has observed an increasing complaint trend on the following failure modes occurring on Arjo medical beds assembled with the Indigo modules: unanticipated device self-acceleration while being operated by a caregiver, unexpected movement without any intentional activation from a stationary position, device movement in a wrong direction (i.e. Backwards instead of forwards and vice versa). Recall Start Date: August 23, 2023 Published 2023-09-08.
What to do now
Contact the manufacturer if you require additional information.
Recall number
74242
Official notice
2023-09-08
The hazard
The hazard
Arjo has observed an increasing complaint trend on the following failure modes occurring on Arjo medical beds assembled with the Indigo modules: unanticipated device self-acceleration while being operated by a caregiver, unexpected movement without any intentional activation from a stationary position, device movement in a wrong direction (i.e. Backwards instead of forwards and vice versa). Recall Start Date: August 23, 2023
How to check if you're affected
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
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Affected products
Product 1
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Arjohuntleigh, Enterprise 9000x With Indigo Module.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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