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Philips lung suite bundles
Official notice
17 Jun 2024
Last checked
17 Jun 2024
An official Health Canada notice concerns Philips lung suite bundles. The lung suite bundles, i.e., lung advanced, lung premium, have been promoted for use for bronchoscopy procedures, while some of the individual medical devices in the relevant bundles are not approved for use for bronchoscopy procedures, but advertised as such. Recall start date: May 29, 2024 Published 2024-06-17.
What to do now
Contact the manufacturer if you require additional information.
Recall number
75682
Official notice
2024-06-17
The hazard
The hazard
The lung suite bundles, i.e., lung advanced, lung premium, have been promoted for use for bronchoscopy procedures, while some of the individual medical devices in the relevant bundles are not approved for use for bronchoscopy procedures, but advertised as such. Recall start date: May 29, 2024
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
Product 2
Product 3
Product 4
Product 5
Product 6
Product 7
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: Philips.
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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