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Siemens Dimension Vista IRON Flex reagent cartridges - safety alert

Official notice

23 Nov 2016

Last checked

23 Nov 2016

Low riskFDA

An official FDA notice concerns Siemens Dimension Vista IRON Flex reagent cartridges - safety alert. An official FDA notice concerns Dimension Vista IRON Flex reagent cartridges. The notice reports a health risk requiring medical assessment. Follow the official notice for consumer instructions. Published 2016-11-23. Lots: 15244AB. Recall numbers: Z-0401-2017. Check the official notice for the complete list. Published 2016-11-23.

What to do now

The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.

Units affected

30,247

Recall number

Z-0401-2017

Official notice

2016-11-23

The hazard

An official FDA notice concerns Dimension Vista IRON Flex reagent cartridges. The notice reports a health risk requiring medical assessment. Follow the official notice for consumer instructions. Published 2016-11-23. Lots: 15244AB. Recall numbers: Z-0401-2017. Check the official notice for the complete list.

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.

Lots

15244AB

Event Ids

75256

Recall Numbers

Z-0401-2017

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Affected products

Product 1

Dimension Vista IRON Flex reagent cartridges

Units affected

30,247

Risk / hazard

An official FDA notice concerns Dimension Vista IRON Flex reagent cartridges. The notice reports a health risk requiring medical assessment. Follow the official notice for consumer instructions. Published 2016-11-23. Lots: 15244AB. Recall numbers: Z-0401-2017. Check the official notice for the complete list.

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

US · United States · DE · Newark

Affected area 1

US · United States · DE · Newark

Affected area 2

US · United States

Company & contacts

Brand

Manufacturer

Not provided

Phone

Not provided

Brand: Siemens. Contact: Siemens Healthcare Diagnostics, Inc..

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

low

Recall details

Recall number

Z-0401-2017

Event id

75256

Units affected

30,247

Status

terminated

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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