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St Jude Medical Proclaim DRG Implantable Pulse Generator, Model Number 3664 - safety alert
Official notice
4 Apr 2018
Last checked
4 Apr 2018
An official FDA notice concerns St Jude Medical Proclaim DRG Implantable Pulse Generator, Model Number 3664 - safety alert. An official FDA notice concerns Proclaim DRG Implantable Pulse Generator, Model Number 3664. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2018-04-04. Lots: 6210849, 6210852, 6499208, 6263128, 6268723 and 1 more. Recall numbers: Z-1170-2018. Check the official notice for the complete list. Published 2018-04-04.
What to do now
The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.
Units affected
17
Recall number
Z-1170-2018
Official notice
2018-04-04
The hazard
The hazard
An official FDA notice concerns Proclaim DRG Implantable Pulse Generator, Model Number 3664. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2018-04-04. Lots: 6210849, 6210852, 6499208, 6263128, 6268723 and 1 more. Recall numbers: Z-1170-2018. 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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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: St Jude Medical. Contact: St. Jude Medical, Inc..
Source & status
Source & status
Recall details
Recall details
Recall number
Event id
Units affected
Status
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Documents, notices & source
See the official notice and source documents for full details.
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