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Micro Therapeutics Pipeline Flex Embolization Device - safety alert
Official notice
15 Sept 2021
Last checked
15 Sept 2021
An official FDA notice concerns Micro Therapeutics Pipeline Flex Embolization Device - safety alert. An official FDA notice concerns Pipeline Flex Embolization Device. The notice reports an injury risk. Stop using the product and follow the official notice. Published 2021-09-15. Lots: A815698, A813323, A822949, A867848, A867214 and 75 more. Recall numbers: Z-2402-2021. Check the official notice for the complete list. Published 2021-09-15.
What to do now
The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.
Units affected
16,169
Recall number
Z-2402-2021
Official notice
2021-09-15
The hazard
The hazard
An official FDA notice concerns Pipeline Flex Embolization Device. The notice reports an injury risk. Stop using the product and follow the official notice. Published 2021-09-15. Lots: A815698, A813323, A822949, A867848, A867214 and 75 more. Recall numbers: Z-2402-2021. 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: Micro Therapeutics. Contact: Micro Therapeutics 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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