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Carefusion 303 CareFusion Alaris PCA Module, Model 8120 - safety alert
Official notice
11 Mar 2020
Last checked
11 Mar 2020
An official FDA notice concerns Carefusion 303 CareFusion Alaris PCA Module, Model 8120 - safety alert. An official FDA notice concerns CareFusion Alaris PCA Module, Model 8120. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2020-03-11. Recall numbers: Z-1362-2020. Check the official notice for the complete list. Published 2020-03-11.
What to do now
The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.
Units affected
83,015
Recall number
Z-1362-2020
Official notice
2020-03-11
The hazard
The hazard
An official FDA notice concerns CareFusion Alaris PCA Module, Model 8120. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2020-03-11. Recall numbers: Z-1362-2020. Check the official notice for the complete list.
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.
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Affected products
Product 1
Units affected
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
Affected area 2
Company & contacts
Company & contacts
Brand: Carefusion 303. Contact: CareFusion 303, Inc..
Source & status
Source & status
Recall details
Recall details
Recall number
Event id
Units affected
Status
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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