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Arrow Radial Artery Catheterization Kit; Model: AK-04120 - safety alert
Official notice
11 Apr 2018
Last checked
11 Apr 2018
An official FDA notice concerns Arrow Radial Artery Catheterization Kit; Model: AK-04120 - safety alert. An official FDA notice concerns Radial Artery Catheterization Kit; Model: AK-04120. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2018-04-11. Recall numbers: Z-1284-2018. Check the official notice for the complete list. Published 2018-04-11.
What to do now
The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.
Units affected
2,491
Recall number
Z-1284-2018
Official notice
2018-04-11
The hazard
The hazard
An official FDA notice concerns Radial Artery Catheterization Kit; Model: AK-04120. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2018-04-11. Recall numbers: Z-1284-2018. 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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Turn on recall alertsAffected products
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: Arrow. Contact: Arrow International 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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